Plants having altered growth and/or development resulted from modulated expression of ubiquitin-specific proteases and a method for making the same

ABSTRACT

The present invention relates generally to the field of molecular biology and concerns a method for altering various aspects of plant growth and/or development by modulating expression in a plant of a nucleic acid encoding an UBiquitin-Specific Protease (UBP) of the UBP15 subfamily or a homologue thereof. The present invention also concerns plants having modulated expression of a nucleic acid encoding a UBP15 or a homologue thereof, which plants have altered growth and/or development relative to corresponding wild type plants or other control plants. The invention also provides constructs useful in the methods of the invention.

RELATED APPLICATIONS

This application is a national stage application (under 35 U.S.C. §371) of PCT/IB2009/050372, filed Jan. 30, 2009, is a continuation-in-part of PCT application PCT/CN2008/000245, filed Jan. 31, 2008.

SUBMISSION OF SEQUENCE LISTING

The sequence Listing with this application is filed in electronic format via EFS-Web and hereby incorporated by reference into the specification in its entirety. The name of the text file containing the Sequence Listing is Sequence₁₃List₁₃12810₁₃01048₁₃US. The size of the text file is 127 KB, and the text file was created on Jul. 23, 2010.

The present invention relates generally to the field of molecular biology and concerns a method for altering various aspects of plant growth and/or development by modulating expression in a plant of a nucleic acid encoding an UBiquitin-Specific Protease (UBP) of the UBP15 subfamily or a homologue thereof. The present invention also concerns plants having modulated expression of a nucleic acid encoding such a UBP15 polypeptide or a homologue thereof, which plants have altered growth and/or development relative to corresponding wild type plants or other control plants. The invention also provides constructs useful in the methods of the invention.

The ever-increasing world population and the dwindling supply of arable land available for agriculture fuels research towards increasing the efficiency of agriculture. Conventional means for crop and horticultural improvements utilise selective breeding techniques to identify plants having desirable characteristics. However, such selective breeding techniques have several drawbacks, namely that these techniques are typically labour intensive and result in plants that often contain heterogeneous genetic components that may not always result in the desirable trait being passed on from parent plants. Advances in molecular biology have allowed mankind to modify the germplasm of animals and plants. Genetic engineering of plants entails the isolation and manipulation of genetic material (typically in the form of DNA or RNA) and the subsequent introduction of that genetic material into a plant. Such technology has the capacity to deliver crops or plants having various improved economic, agronomic or horticultural traits.

It has now been found that plant growth and/or development may be altered by modulating expression in a plant of a nucleic acid encoding a UBP15 polypeptide or a homologue thereof.

BACKGROUND

Ubiquitin-Specific Proteases (UBPs) are a conserved family of proteins in eukaryotes that play critical roles in protein de-ubiquitination. The covalent modification of proteins by ubiquitin play a central role in diverse cellular pathways such as cell cycle progression, signal transduction, transcriptional regulation, DNA repair, stress responses, endocytosis and apoptosis (Hochstrasser, 1996; Varshaysky, 1997; Hershko and Ciechanover, 1998; Weissman, 2001; Pickart, 2004). Protein ubiquitination is catalyzed by a cascade of three enzymes. Ubiquitn is first activated by ubiquitin-activating enzyme (E1), which forms a thiolester bond with the ubiquitin C-terminus. Ubiquitin is then transferred to ubiquitin-conjugating enzyme (E2). Although some E2s can catalyze ligation of the ubiquitin C-terminus to the lysine residue of target proteins with the aid of ubiquitin ligases (E3s), other E2s transfer their conjugated ubiquitin to E3s before targetting to substrates. Target substrate proteins can be mono-ubiquitinated or multi-ubiquitinated by successive conjugation of the ubiquitin C-terminus to the lysine residue of the prior one through several possible linkages. The fate of ubiquitinated substrate proteins depends in part on the number of conjugated ubiquitin(s) and on the mode of linkage in the ubiquitin chain. The most common ubiquitination is multi-ubiquitin chain (ubiquitin number>=4) linked by Lys48, acting as a signal for protein degradation by 26S proteasome.

Cleavage of ubiquitin from proteins by de-ubiquitination enzymes (DUBs) can also affect the ubiquitinated substrate protein's activity and fate (Wilkinson, 1997; Amerik and Hochstrasser, 2004; Crosas et al., 2006; Hanna et al., 2006). Those DUBs are proteases that specifically cleave the peptide bond between ubiquitins or between the C-terminus of ubiquitin and covalently attached polypeptides. The currently known DUBs together carry out four types of essential biochemical functions: first, they generate mature ubiquitins from ubiquitin precursors (fused to ribosomal protein) and polyubiquitin gene products; secondly, they rescue proteins that are inappropriately ubiquitinated; thirdly, they cleave ubiquitin (chains) from attached substrate proteins; and fourth, release free ubiquitin monomers from multi-ubiquitin chains. The last three roles are accompanied by cleavage of the isopeptide bonds between the ubiquitin C-terminus Gly and Lys ε-amino residue of a target protein.

Cysteine proteases and metalloproteases are the two major groups of the DUB superfamily, with cysteine proteases being most numerous in eukaryotes (Nijman et al., 2005). All known metalloproteases have a JAMM domain for catalytic activity (Verma et al., 2002). The cysteine protease DUBs can be further divided into four families based on the organization of ubiquitin-protease catalytic center structure and organization (Wilkinson, 1997; Amerik and Hochstrasser, 2004; Nijman et al., 2005). Ubiquitin-Specific Proteases (UBP, or USPs as defined in mammals) possess catalytic triad residues in highly conserved cysteine box and histidine box (Hu et al., 2002). Ubiquitin C-terminal Hydrolases (UCHs), with similar catalytic triad residues in two conserved cysteine and histidine boxes (Johnston et al., 1997; Johnston et al., 1999), have a smaller overall protein size as well as a structural obstacle over the catalytic surface to restrict their ability to hydrolyze only small amides and esters at the C-terminus of ubiquitin (Amerik and Hochstrasser, 2004). Ovarian Tumor Proteases (OTUs) have a catalytic triad comparable to above two families in Cysteine and Histidine boxes but containing an OTU-related motif and being considered as a part of UBP family (Balakirev et al., 2003; Nanao et al., 2004). Lastly, Machado-Joseph Disease Protein Domain Proteases (MJDs) possess a cysteine and histidine box-like domain but with rather low sequence similarity to the other three groups (Burnett et al., 2003; Scheel et al., 2003). The UBP family makes up the bulk of the cysteine proteases. All four types of the above mentioned DUB biochemical functions are found in UBPs family, while UCHs only perform their functions on small proteins and ubiquitin precursor.

In the model plant Arabidopsis thaliana, an in silico analysis of the completely sequenced genome revealed a total of 27 UBPs based on the presence of the conserved Cys and His boxes; those 27 UBPs were further divided into 14 subfamilies (Yan et al., 2000). Previous reports showed that UBP3 and UBP4 constitute one subfamily, possess UBP activity in vitro and are present in the nucleus (Chandler et al., 1997; Rao-Naik et al., 2000). Another member, UBP5, was shown also to have de-ubiquitination activity in vitro (Rao-Naik et al., 2000). A genetic analysis of UBP1 and UBP2, members of another subfamily, were reported to be required for resistance to the amino acid analog canavanine (Yan et al., 2000). Furthermore, a loss-of-function mutation in UBP14 was shown to be lethal in early embryo development (Doelling et al., 2001).

SUMMARY

Surprisingly, it has now been found that modulating expression of a nucleic acid encoding a UBP15 polypeptide or a homologue thereof gives plants altered growth and/or development relative to control plants.

According one embodiment, there is provided a method for altering plant growth and/or development relative to control plants, comprising modulating expression in a plant of a nucleic acid encoding a UBP15 polypeptide or a homologue thereof.

DEFINITIONS

Polypeptide(s)/Protein(s)

The terms “polypeptide” and “protein” are used interchangeably herein and refer to amino acids in a polymeric form of any length, linked together by peptide bonds.

Polynucleotide(s)/Nucleic Acid(s)/Nucleic Acid Sequence(s)/Nucleotide Sequence(s)

The terms “polynucleotide(s)”, “nucleic acid sequence(s)”, “nucleotide sequence(s)”, “nucleic acid(s)”, “nucleic acid molecule” are used interchangeably herein and refer to nucleotides, either ribonucleotides or deoxyribonucleotides or a combination of both, in a polymeric unbranched form of any length.

Control Plant(s)

The choice of suitable control plants is a routine part of an experimental setup and may include corresponding wild type plants or corresponding plants without the gene of interest. The control plant is typically of the same plant species or even of the same variety as the plant to be assessed. The control plant may also be a nullizygote of the plant to be assessed. Nullizygotes are individuals missing the transgene by segregation. A “control plant” as used herein refers not only to whole plants, but also to plant parts, including seeds and seed parts.

Homoloque(s)

“Homologues” of a protein encompass peptides, oligopeptides, polypeptides, proteins and enzymes having amino acid substitutions, deletions and/or insertions relative to the unmodified protein in question and having similar biological and functional activity as the unmodified protein from which they are derived.

A deletion refers to removal of one or more amino acids from a protein.

An insertion refers to one or more amino acid residues being introduced into a predetermined site in a protein. Insertions may comprise N-terminal and/or C-terminal fusions as well as intra-sequence insertions of single or multiple amino acids. Generally, insertions within the amino acid sequence will be smaller than N- or C-terminal fusions, of the order of about 1 to 10 residues. Examples of N- or C-terminal fusion proteins or peptides include the binding domain or activation domain of a transcriptional activator as used in the yeast two-hybrid system, phage coat proteins, (histidine)-6-tag, glutathione S-transferase-tag, protein A, maltose-binding protein, dihydrofolate reductase, Tag·100 epitope, c-myc epitope, FLAG®-epitope, lacZ, CMP (calmodulin-binding peptide), HA epitope, protein C epitope and VSV epitope.

A substitution refers to replacement of amino acids of the protein with other amino acids having similar properties (such as similar hydrophobicity, hydrophilicity, antigenicity, propensity to form or break α-helical structures or β-sheet structures). Amino acid substitutions are typically of single residues, but may be clustered depending upon functional constraints placed upon the polypeptide; insertions will usually be of the order of about 1 to 10 amino acid residues. The amino acid substitutions are preferably conservative amino acid substitutions. Conservative substitution tables are well known in the art (see for example Creighton (1984) Proteins. W.H. Freeman and Company (Eds) and Table A below).

TABLE A Examples of conserved amino acid substitutions Conservative Residue Substitutions Ala Ser Arg Lys Asn Gln; His Asp Glu Gln Asn Cys Ser Glu Asp Gly Pro His Asn; Gln Ile Leu, Val Leu Ile; Val Lys Arg; Gln Met Leu; Ile Phe Met; Leu; Tyr Ser Thr; Gly Thr Ser; Val Trp Tyr Tyr Trp; Phe Val Ile; Leu

Amino acid substitutions, deletions and/or insertions may readily be made using peptide synthetic techniques well known in the art, such as solid phase peptide synthesis and the like, or by recombinant DNA manipulation. Methods for the manipulation of DNA sequences to produce substitution, insertion or deletion variants of a protein are well known in the art. For example, techniques for making substitution mutations at predetermined sites in DNA are well known to those skilled in the art and include M13 mutagenesis, T7-Gen in vitro mutagenesis (USB, Cleveland, Ohio), QuickChange Site Directed mutagenesis (Stratagene, San Diego, Calif.), PCR-mediated site-directed mutagenesis or other site-directed mutagenesis protocols.

Derivatives

“Derivatives” include peptides, oligopeptides, polypeptides which may, compared to the amino acid sequence of the naturally-occurring form of the protein, such as the protein of interest, comprise substitutions of amino acids with non-naturally occurring amino acid residues, or additions of non-naturally occurring amino acid residues. “Derivatives” of a protein also encompass peptides, oligopeptides, polypeptides which comprise naturally occurring altered (glycosylated, acylated, prenylated, phosphorylated, myristoylated, sulphated etc.) or non-naturally altered amino acid residues compared to the amino acid sequence of a naturally-occurring form of the polypeptide. A derivative may also comprise one or more non-amino acid substituents or additions compared to the amino acid sequence from which it is derived, for example a reporter molecule or other ligand, covalently or non-covalently bound to the amino acid sequence, such as a reporter molecule which is bound to facilitate its detection, and non-naturally occurring amino acid residues relative to the amino acid sequence of a naturally-occurring protein. Furthermore, “derivatives” also include fusions of the naturally-occurring form of the protein with tagging peptides such as FLAG, HIS6 or thioredoxin (for a review of tagging peptides, see Terpe, Appl. Microbiol. Biotechnol. 60, 523-533, 2003).

Ortholoque(s)/Paraloque(s)

Orthologues and paralogues encompass evolutionary concepts used to describe the ancestral relationships of genes. Paralogues are genes within the same species that have originated through duplication of an ancestral gene; orthologues are genes from different organisms that have originated through speciation, and are also derived from a common ancestral gene.

Domain

The term “domain” refers to a set of amino acids conserved at specific positions along an alignment of sequences of evolutionarily related proteins. While amino acids at other positions can vary between homologues, amino acids that are highly conserved at specific positions indicate amino acids that are likely essential in the structure, stability or function of a protein. Identified by their high degree of conservation in aligned sequences of a family of protein homologues, they can be used as identifiers to determine if any polypeptide in question belongs to a previously identified polypeptide family.

Motif/Consensus Sequence/Signature

The term “motif” or “consensus sequence” or “signature” refers to a short conserved region in the sequence of evolutionarily related proteins. Motifs are frequently highly conserved parts of domains, but may also include only part of the domain, or be located outside of conserved domain (if all of the amino acids of the motif fall outside of a defined domain).

Hybridisation

The term “hybridisation” as defined herein is a process wherein substantially homologous complementary nucleotide sequences anneal to each other. The hybridisation process can occur entirely in solution, i.e. both complementary nucleic acids are in solution. The hybridisation process can also occur with one of the complementary nucleic acids immobilised to a matrix such as magnetic beads, Sepharose beads or any other resin. The hybridisation process can furthermore occur with one of the complementary nucleic acids immobilised to a solid support such as a nitro-cellulose or nylon membrane or immobilised by e.g. photolithography to, for example, a siliceous glass support (the latter known as nucleic acid arrays or microarrays or as nucleic acid chips). In order to allow hybridisation to occur, the nucleic acid molecules are generally thermally or chemically denatured to melt a double strand into two single strands and/or to remove hairpins or other secondary structures from single stranded nucleic acids.

The term “stringency” refers to the conditions under which a hybridisation takes place. The stringency of hybridisation is influenced by conditions such as temperature, salt concentration, ionic strength and hybridisation buffer composition. Generally, low stringency conditions are selected to be about 30° C. lower than the thermal melting point (T_(m)) for the specific sequence at a defined ionic strength and pH. Medium stringency conditions are when the temperature is 20° C. below T_(m), and high stringency conditions are when the temperature is 10° C. below T_(m). High stringency hybridisation conditions are typically used for isolating hybridising sequences that have high sequence similarity to the target nucleic acid sequence. However, nucleic acids may deviate in sequence and still encode a substantially identical polypeptide, due to the degeneracy of the genetic code. Therefore medium stringency hybridisation conditions may sometimes be needed to identify such nucleic acid molecules.

The Tm is the temperature under defined ionic strength and pH, at which 50% of the target sequence hybridises to a perfectly matched probe. The T_(m) is dependent upon the solution conditions and the base composition and length of the probe. For example, longer sequences hybridise specifically at higher temperatures. The maximum rate of hybridisation is obtained from about 16° C. up to 32° C. below T_(m). The presence of monovalent cations in the hybridisation solution reduce the electrostatic repulsion between the two nucleic acid strands thereby promoting hybrid formation; this effect is visible for sodium concentrations of up to 0.4M (for higher concentrations, this effect may be ignored). Formamide reduces the melting temperature of DNA-DNA and DNA-RNA duplexes with 0.6 to 0.7° C. for each percent formamide, and addition of 50% formamide allows hybridisation to be performed at 30 to 45° C., though the rate of hybridisation will be lowered. Base pair mismatches reduce the hybridisation rate and the thermal stability of the duplexes. On average and for large probes, the Tm decreases about 1° C. per % base mismatch. The Tm may be calculated using the following equations, depending on the types of hybrids:

-   1) DNA-DNA hybrids (Meinkoth and Wahl, Anal. Biochem., 138: 267-284,     1984):     -   T_(m)=81.5°         C.+16.6×log₁₀[Na⁺]^(a)+0.41×%[G/C^(b)]−500x[L^(c)]⁻¹−0.61×%         formamide -   2) DNA-RNA or RNA-RNA hybrids:     -   Tm=79.8+18.5 (log₁₀[Na⁺]^(a))+0.58 (% G/C^(b))+11.8 (%         G/C^(b))²−820/L^(c) -   3) oligo-DNA or oligo-RNA^(d) hybrids:     -   For <20 nucleotides: T_(m)=2 (I_(n))     -   For 20-35 nucleotides: T_(m)=22+1.46 (I_(n)) ^(a) or for other         monovalent cation, but only accurate in the 0.01-0.4 M         range.^(b) only accurate for % GC in the 30% to 75% range.^(c)         L=length of duplex in base pairs.^(d) oligo, oligonucleotide;         I_(n),=effective length of primer=2×(no. of G/C)+(no. of A/T).

Non-specific binding may be controlled using any one of a number of known techniques such as, for example, blocking the membrane with protein containing solutions, additions of heterologous RNA, DNA, and SDS to the hybridisation buffer, and treatment with Rnase. For non-homologous probes, a series of hybridizations may be performed by varying one of (i) progressively lowering the annealing temperature (for example from 68° C. to 42° C.) or (ii) progressively lowering the formamide concentration (for example from 50% to 0%). The skilled artisan is aware of various parameters which may be altered during hybridisation and which will either maintain or change the stringency conditions.

Besides the hybridisation conditions, specificity of hybridisation typically also depends on the function of post-hybridisation washes. To remove background resulting from non-specific hybridisation, samples are washed with dilute salt solutions. Critical factors of such washes include the ionic strength and temperature of the final wash solution: the lower the salt concentration and the higher the wash temperature, the higher the stringency of the wash. Wash conditions are typically performed at or below hybridisation stringency. A positive hybridisation gives a signal that is at least twice of that of the background. Generally, suitable stringent conditions for nucleic acid hybridisation assays or gene amplification detection procedures are as set forth above. More or less stringent conditions may also be selected. The skilled artisan is aware of various parameters which may be altered during washing and which will either maintain or change the stringency conditions.

For example, typical high stringency hybridisation conditions for DNA hybrids longer than 50 nucleotides encompass hybridisation at 65° C. in 1×SSC or at 42° C. in 1×SSC and 50% formamide, followed by washing at 65° C. in 0.3×SSC. Examples of medium stringency hybridisation conditions for DNA hybrids longer than 50 nucleotides encompass hybridisation at 50° C. in 4×SSC or at 40° C. in 6×SSC and 50% formamide, followed by washing at 50° C. in 2×SSC. The length of the hybrid is the anticipated length for the hybridising nucleic acid. When nucleic acids of known sequence are hybridised, the hybrid length may be determined by aligning the sequences and identifying the conserved regions described herein. 1×SSC is 0.15M NaCl and 15 mM sodium citrate; the hybridisation solution and wash solutions may additionally include 5× Denhardt's reagent, 0.5-1.0% SDS, 100 μg/ml denatured, fragmented salmon sperm DNA, 0.5% sodium pyrophosphate.

For the purposes of defining the level of stringency, reference can be made to Sambrook et al. (2001) Molecular Cloning: a laboratory manual, 3^(rd) Edition, Cold Spring Harbor Laboratory Press, CSH, New York or to Current Protocols in Molecular Biology, John Wiley & Sons, N.Y. (1989 and yearly updates).

Splice Variant

The term “splice variant” as used herein encompasses variants of a nucleic acid sequence in which selected introns and/or exons have been excised, replaced, displaced or added, or in which introns have been shortened or lengthened. Such variants will be ones in which the biological activity of the protein is substantially retained; this may be achieved by selectively retaining functional segments of the protein. Such splice variants may be found in nature or may be manmade. Methods for predicting and isolating such splice variants are well known in the art (see for example Foissac and Schiex (2005) BMC Bioinformatics 6: 25).

Allelic Variant

Alleles or allelic variants are alternative forms of a given gene, located at the same chromosomal position. Allelic variants encompass Single Nucleotide Polymorphisms (SNPs), as well as Small Insertion/Deletion Polymorphisms (INDELs). The size of INDELs is usually less than 100 bp. SNPs and INDELs form the largest set of sequence variants in naturally occurring polymorphic strains of most organisms.

Gene Shuffling/Directed Evolution

Gene shuffling or directed evolution consists of iterations of DNA shuffling followed by appropriate screening and/or selection to generate variants of nucleic acids or portions thereof encoding proteins having a modified biological activity (Castle et al., (2004) Science 304(5674): 1151-4; U.S. Pat. Nos. 5,811,238 and 6,395,547).

Regulatory Element/Control Sequence/Promoter

The terms “regulatory element”, “control sequence” and “promoter” are all used interchangeably herein and are to be taken in a broad context to refer to regulatory nucleic acid sequences capable of effecting expression of the sequences to which they are ligated. The term “promoter” typically refers to a nucleic acid control sequence located upstream from the transcriptional start of a gene and which is involved in recognising and binding of RNA polymerase and other proteins, thereby directing transcription of an operably linked nucleic acid. Encompassed by the aforementioned terms are transcriptional regulatory sequences derived from a classical eukaryotic genomic gene (including the TATA box which is required for accurate transcription initiation, with or without a CCAAT box sequence) and additional regulatory elements (i.e. upstream activating sequences, enhancers and silencers) which alter gene expression in response to developmental and/or external stimuli, or in a tissue-specific manner. Also included within the term is a transcriptional regulatory sequence of a classical prokaryotic gene, in which case it may include a −35 box sequence and/or −10 box transcriptional regulatory sequences. The term “regulatory element” also encompasses a synthetic fusion molecule or derivative that confers, activates or enhances expression of a nucleic acid molecule in a cell, tissue or organ.

A “plant promoter” comprises regulatory elements, which mediate the expression of a coding sequence segment in plant cells. Accordingly, a plant promoter need not be of plant origin, but may originate from viruses or micro-organisms, for example from viruses which attack plant cells. The “plant promoter” can also originate from a plant cell, e.g. from the plant which is transformed with the nucleic acid sequence to be expressed in the inventive process and described herein. This also applies to other “plant” regulatory signals, such as “plant” terminators. The promoters upstream of the nucleotide sequences useful in the methods of the present invention can be modified by one or more nucleotide substitution(s), insertion(s) and/or deletion(s) without interfering with the functionality or activity of either the promoters, the open reading frame (ORF) or the 3′-regulatory region such as terminators or other 3′ regulatory regions which are located away from the ORF. It is furthermore possible that the activity of the promoters is increased by modification of their sequence, or that they are replaced completely by more active promoters, even promoters from heterologous organisms. For expression in plants, the nucleic acid molecule must, as described above, be linked operably to or comprise a suitable promoter which expresses the gene at the right point in time and with the required spatial expression pattern.

For the identification of functionally equivalent promoters, the promoter strength and/or expression pattern of a candidate promoter may be analysed for example by operably linking the promoter to a reporter gene and assaying the expression level and pattern of the reporter gene in various tissues of the plant. Suitable well-known reporter genes include for example beta-glucuronidase or beta-galactosidase. The promoter activity is assayed by measuring the enzymatic activity of the beta-glucuronidase or beta-galactosidase. The promoter strength and/or expression pattern may then be compared to that of a reference promoter (such as the one used in the methods of the present invention). Alternatively, promoter strength may be assayed by quantifying mRNA levels or by comparing mRNA levels of the nucleic acid used in the methods of the present invention, with mRNA levels of housekeeping genes such as 18S rRNA, using methods known in the art, such as Northern blotting with densitometric analysis of autoradiograms, quantitative real-time PCR or RT-PCR (Heid et al., 1996 Genome Methods 6: 986-994). Generally by “weak promoter” is intended a promoter that drives expression of a coding sequence at a low level. By “low level” is intended at levels of about 1/10,000 transcripts to about 1/100,000 transcripts, to about 1/500,0000 transcripts per cell. Conversely, a “strong promoter” drives expression of a coding sequence at high level, or at about 1/10 transcripts to about 1/100 transcripts to about 1/1000 transcripts per cell.

Operably Linked

The term “operably linked” as used herein refers to a functional linkage between the promoter sequence and the gene of interest, such that the promoter sequence is able to initiate transcription of the gene of interest.

Constitutive Promoter

A “constitutive promoter” refers to a promoter that is transcriptionally active during most, but not necessarily all, phases of growth and development and under most environmental conditions, in at least one cell, tissue or organ. Table B below gives examples of constitutive promoters.

TABLE B Examples of constitutive promoters Gene Source Reference Actin McElroy et al, Plant Cell, 2: 163-171, 1990 HMGP WO 2004/070039 CAMV 35S Odell et al, Nature, 313: 810-812, 1985 CaMV 19S Nilsson et al., Physiol. Plant. 100: 456-462, 1997 GOS2 de Pater et al, Plant J Nov; 2(6): 837-44, 1992, WO 2004/065596 Ubiquitin Christensen et al, Plant Mol. Biol. 18: 675-689, 1992 Rice cyclophilin Buchholz et al, Plant Mol Biol. 25(5): 837-43, 1994 Maize H3 histone Lepetit et al, Mol. Gen. Genet. 231: 276-285, 1992 Alfalfa H3 histone Wu et al. Plant Mol. Biol. 11: 641-649, 1988 Actin 2 An et al, Plant J. 10(1); 107-121, 1996 34S FMV Sanger et al., Plant. Mol. Biol., 14, 1990: 433-443 Rubisco small U.S. Pat. No. 4,962,028 subunit OCS Leisner (1988) Proc Natl Acad Sci USA 85(5): 2553 SAD1 Jain et al., Crop Science, 39 (6), 1999: 1696 SAD2 Jain et al., Crop Science, 39 (6), 1999: 1696 Nos Shaw et al. (1984) Nucleic Acids Res. 12(20): 7831-7846 V-ATPase WO 01/14572 Super promoter WO 95/14098 G-box proteins WO 94/12015 Ubiquitous Promoter

A ubiquitous promoter is active in substantially all tissues or cells of an organism.

Developmentally-Regulated Promoter

A developmentally-regulated promoter is active during certain developmental stages or in parts of the plant that undergo developmental changes.

Inducible Promoter

An inducible promoter has induced or increased transcription initiation in response to a chemical (for a review see Gatz 1997, Annu. Rev. Plant Physiol. Plant Mol. Biol., 48:89-108), environmental or physical stimulus, or may be “stress-inducible”, i.e. activated when a plant is exposed to various stress conditions, or a “pathogen-inducible” i.e. activated when a plant is exposed to exposure to various pathogens.

Organ-Specific/Tissue-Specific Promoter

An organ-specific or tissue-specific promoter is one that is capable of preferentially initiating transcription in certain organs or tissues, such as the leaves, roots, seed tissue etc. For example, a “root-specific promoter” is a promoter that is transcriptionally active predominantly in plant roots, substantially to the exclusion of any other parts of a plant, whilst still allowing for any leaky expression in these other plant parts. Promoters able to initiate transcription in certain cells only are referred to herein as “cell-specific”.

A seed-specific promoter is transcriptionally active predominantly in seed tissue, but not necessarily exclusively in seed tissue (in cases of leaky expression). The seed-specific promoter may be active during seed development and/or during germination. The seed specific promoter may be endosperm and/or aleurone and/or embryo-specific.

Terminator

The term “terminator” encompasses a control sequence which is a DNA sequence at the end of a transcriptional unit which signals 3′ processing and polyadenylation of a primary transcript and termination of transcription. The terminator can be derived from the natural gene, from a variety of other plant genes, or from T-DNA. The terminator to be added may be derived from, for example, the nopaline synthase or octopine synthase genes, or alternatively from another plant gene, or less preferably from any other eukaryotic gene.

Modulation

The term “modulation” means in relation to expression or gene expression, a process in which the expression level is changed by said gene expression in comparison to the control plant, the expression level may be increased or decreased. The original, unmodulated expression may be of any kind of expression of a structural RNA (rRNA, tRNA) or mRNA with subsequent translation.

Expression

The term “expression” or “gene expression” means the transcription of a specific gene or specific genes or specific genetic construct. The term “expression” or “gene expression” in particular means the transcription of a gene or genes or genetic construct into structural RNA (rRNA, tRNA) or mRNA with or without subsequent translation of the latter into a protein. The process includes transcription of DNA and processing of the resulting mRNA product.

Increased Expression/Overexpression

The term “increased expression” or “overexpression” as used herein means any form of expression that is additional to the original wild-type expression level.

Methods for increasing expression of genes or gene products are well documented in the art and include, for example, overexpression driven by appropriate promoters, the use of transcription enhancers or translation enhancers. Isolated nucleic acids which serve as promoter or enhancer elements may be introduced in an appropriate position (typically upstream) of a non-heterologous form of a polynucleotide so as to upregulate expression of a nucleic acid encoding the polypeptide of interest. For example, endogenous promoters may be altered in vivo by mutation, deletion, and/or substitution (see, Kmiec, U.S. Pat. No. 5,565,350; Zarling et al., WO9322443), or isolated promoters may be introduced into a plant cell in the proper orientation and distance from a gene of the present invention so as to control the expression of the gene.

If polypeptide expression is desired, it is generally desirable to include a polyadenylation region at the 3′-end of a polynucleotide coding region. The polyadenylation region can be derived from the natural gene, from a variety of other plant genes, or from T-DNA. The 3′ end sequence to be added may be derived from, for example, the nopaline synthase or octopine synthase genes, or alternatively from another plant gene, or less preferably from any other eukaryotic gene.

An intron sequence may also be added to the 5′ untranslated region (UTR) or the coding sequence of the partial coding sequence to increase the amount of the mature message that accumulates in the cytosol. Inclusion of a spliceable intron in the transcription unit in both plant and animal expression constructs has been shown to increase gene expression at both the mRNA and protein levels up to 1000-fold (Buchman and Berg (1988) Mol. Cell biol. 8: 4395-4405; Callis et al. (1987) Genes Dev 1:1183-1200). Such intron enhancement of gene expression is typically greatest when placed near the 5′ end of the transcription unit. Use of the maize introns Adh1-S intron 1, 2, and 6, the Bronze-1 intron are known in the art. For general information see: The Maize Handbook, Chapter 116, Freeling and Walbot, Eds., Springer, N.Y. (1994).

Endogenous Gene

Reference herein to an “endogenous” gene not only refers to the gene in question as found in a plant in its natural form (i.e., without there being any human intervention), but also refers to that same gene (or a substantially homologous nucleic acid/gene) in an isolated form subsequently (re)introduced into a plant (a transgene). For example, a transgenic plant containing such a transgene may encounter a substantial reduction of the transgene expression and/or substantial reduction of expression of the endogenous gene. The isolated gene may be isolated from an organism or may be manmade, for example by chemical synthesis.

Decreased Expression

Reference herein to “decrease depression” or “reduction or substantial elimination” of expression is taken to mean a decrease in endogenous gene expression and/or polypeptide levels and/or polypeptide activity relative to control plants. The reduction or substantial elimination is in increasing order of preference at least 10%, 20%, 30%, 40% or 50%, 60%, 70%, 80%, 85%, 90%, or 95%, 96%, 97%, 98%, 99% or more reduced compared to that of control plants.

For the reduction or substantial elimination of expression an endogenous gene in a plant, a sufficient length of substantially contiguous nucleotides of a nucleic acid sequence is required. In order to perform gene silencing, this may be as little as 20, 19, 18, 17, 16, 15, 14, 13, 12, 11, 10 or fewer nucleotides, alternatively this may be as much as the entire gene (including the 5′ and/or 3′ UTR, either in part or in whole). The stretch of substantially contiguous nucleotides may be derived from the nucleic acid encoding the protein of interest (target gene), or from any nucleic acid capable of encoding an orthologue, paralogue or homologue of the protein of interest. Preferably, the stretch of substantially contiguous nucleotides is capable of forming hydrogen bonds with the target gene (either sense or antisense strand), more preferably, the stretch of substantially contiguous nucleotides has, in increasing order of preference, 50%, 60%, 70%, 80%, 85%, 90%, 95%, 96% 97%, 98%, 99%, 100% sequence identity to the target gene (either sense or antisense strand). A nucleic acid sequence encoding a (functional) polypeptide is not a requirement for the various methods discussed herein for the reduction or substantial elimination of expression of an endogenous gene.

This reduction or substantial elimination of expression may be achieved using routine tools and techniques. A preferred method for the reduction or substantial elimination of endogenous gene expression is by introducing and expressing in a plant a genetic construct into which the nucleic acid (in this case a stretch of substantially contiguous nucleotides derived from the gene of interest, or from any nucleic acid capable of encoding an orthologue, paralogue or homologue of any one of the protein of interest) is cloned as an inverted repeat (in part or completely), separated by a spacer (non-coding DNA).

In such a preferred method, expression of the endogenous gene is reduced or substantially eliminated through RNA-mediated silencing using an inverted repeat of a nucleic acid or a part thereof (in this case a stretch of substantially contiguous nucleotides derived from the gene of interest, or from any nucleic acid capable of encoding an orthologue, paralogue or homologue of the protein of interest), preferably capable of forming a hairpin structure. The inverted repeat is cloned in an expression vector comprising control sequences. A non-coding DNA nucleic acid sequence (a spacer, for example a matrix attachment region fragment (MAR), an intron, a polylinker, etc.) is located between the two inverted nucleic acids forming the inverted repeat. After transcription of the inverted repeat, a chimeric RNA with a self-complementary structure is formed (partial or complete). This double-stranded RNA structure is referred to as the hairpin RNA (hpRNA). The hpRNA is processed by the plant into siRNAs that are incorporated into an RNA-induced silencing complex (RISC). The RISC further cleaves the mRNA transcripts, thereby substantially reducing the number of mRNA transcripts to be translated into polypeptides. For further general details see for example, Grierson et al. (1998) WO 98/53083; Waterhouse et al. (1999) WO 99/53050).

Performance of the methods of the invention does not rely on introducing and expressing in a plant a genetic construct into which the nucleic acid is cloned as an inverted repeat, but any one or more of several well-known “gene silencing” methods may be used to achieve the same effects.

One such method for the reduction of endogenous gene expression is RNA-mediated silencing of gene expression (downregulation). Silencing in this case is triggered in a plant by a double stranded RNA sequence (dsRNA) that is substantially similar to the target endogenous gene. This dsRNA is further processed by the plant into about 20 to about 26 nucleotides called short interfering RNAs (siRNAs). The siRNAs are incorporated into an RNA-induced silencing complex (RISC) that cleaves the mRNA transcript of the endogenous target gene, thereby substantially reducing the number of mRNA transcripts to be translated into a polypeptide. Preferably, the double stranded RNA sequence corresponds to a target gene.

Another example of an RNA silencing method involves the introduction of nucleic acid sequences or parts thereof (in this case a stretch of substantially contiguous nucleotides derived from the gene of interest, or from any nucleic acid capable of encoding an orthologue, paralogue or homologue of the protein of interest) in a sense orientation into a plant. “Sense orientation” refers to a DNA sequence that is homologous to an mRNA transcript thereof. Introduced into a plant would therefore be at least one copy of the nucleic acid sequence. The additional nucleic acid sequence will reduce expression of the endogenous gene, giving rise to a phenomenon known as co-suppression. The reduction of gene expression will be more pronounced if several additional copies of a nucleic acid sequence are introduced into the plant, as there is a positive correlation between high transcript levels and the triggering of co-suppression.

Another example of an RNA silencing method involves the use of antisense nucleic acid sequences. An “antisense” nucleic acid sequence comprises a nucleotide sequence that is complementary to a “sense” nucleic acid sequence encoding a protein, i.e. complementary to the coding strand of a double-stranded cDNA molecule or complementary to an mRNA transcript sequence. The antisense nucleic acid sequence is preferably complementary to the endogenous gene to be silenced. The complementarity may be located in the “coding region” and/or in the “non-coding region” of a gene. The term “coding region” refers to a region of the nucleotide sequence comprising codons that are translated into amino acid residues. The term “non-coding region” refers to 5′ and 3′ sequences that flank the coding region that are transcribed but not translated into amino acids (also referred to as 5′ and 3′ untranslated regions).

Antisense nucleic acid sequences can be designed according to the rules of Watson and Crick base pairing. The antisense nucleic acid sequence may be complementary to the entire nucleic acid sequence (in this case a stretch of substantially contiguous nucleotides derived from the gene of interest, or from any nucleic acid capable of encoding an orthologue, paralogue or homologue of the protein of interest), but may also be an oligonucleotide that is antisense to only a part of the nucleic acid sequence (including the mRNA 5′ and 3′ UTR). For example, the antisense oligonucleotide sequence may be complementary to the region surrounding the translation start site of an mRNA transcript encoding a polypeptide. The length of a suitable antisense oligonucleotide sequence is known in the art and may start from about 50, 45, 40, 35, 30, 25, 20, 15 or 10 nucleotides in length or less. An antisense nucleic acid sequence according to the invention may be constructed using chemical synthesis and enzymatic ligation reactions using methods known in the art. For example, an antisense nucleic acid sequence (e.g., an antisense oligonucleotide sequence) may be chemically synthesized using naturally occurring nucleotides or variously modified nucleotides designed to increase the biological stability of the molecules or to increase the physical stability of the duplex formed between the antisense and sense nucleic acid sequences, e.g., phosphorothioate derivatives and acridine substituted nucleotides may be used. Examples of modified nucleotides that may be used to generate the antisense nucleic acid sequences are well known in the art. Known nucleotide modifications include methylation, cyclization and ‘caps’ and substitution of one or more of the naturally occurring nucleotides with an analogue such as inosine. Other modifications of nucleotides are well known in the art.

The antisense nucleic acid sequence can be produced biologically using an expression vector into which a nucleic acid sequence has been subcloned in an antisense orientation (i.e., RNA transcribed from the inserted nucleic acid will be of an antisense orientation to a target nucleic acid of interest). Preferably, production of antisense nucleic acid sequences in plants occurs by means of a stably integrated nucleic acid construct comprising a promoter, an operably linked antisense oligonucleotide, and a terminator.

The nucleic acid molecules used for silencing in the methods of the invention (whether introduced into a plant or generated in situ) hybridize with or bind to mRNA transcripts and/or genomic DNA encoding a polypeptide to thereby inhibit expression of the protein, e.g., by inhibiting transcription and/or translation. The hybridization can be by conventional nucleotide complementarity to form a stable duplex, or, for example, in the case of an antisense nucleic acid sequence which binds to DNA duplexes, through specific interactions in the major groove of the double helix. Antisense nucleic acid sequences may be introduced into a plant by transformation or direct injection at a specific tissue site. Alternatively, antisense nucleic acid sequences can be modified to target selected cells and then administered systemically. For example, for systemic administration, antisense nucleic acid sequences can be modified such that they specifically bind to receptors or antigens expressed on a selected cell surface, e.g., by linking the antisense nucleic acid sequence to peptides or antibodies which bind to cell surface receptors or antigens. The antisense nucleic acid sequences can also be delivered to cells using the vectors described herein.

According to a further aspect, the antisense nucleic acid sequence is an a-anomeric nucleic acid sequence. An a-anomeric nucleic acid sequence forms specific double-stranded hybrids with complementary RNA in which, contrary to the usual b-units, the strands run parallel to each other (Gaultier et al. (1987) Nucl Ac Res 15: 6625-6641). The antisense nucleic acid sequence may also comprise a 2′-o-methylribonucleotide (Inoue et al. (1987) Nucl Ac Res 15, 6131-6148) or a chimeric RNA-DNA analogue (Inoue et al. (1987) FEBS Lett. 215, 327-330).

The reduction or substantial elimination of endogenous gene expression may also be performed using ribozymes. Ribozymes are catalytic RNA molecules with ribonuclease activity that are capable of cleaving a single-stranded nucleic acid sequence, such as an mRNA, to which they have a complementary region. Thus, ribozymes (e.g., hammerhead ribozymes (described in Haselhoff and Gerlach (1988) Nature 334, 585-591) can be used to catalytically cleave mRNA transcripts encoding a polypeptide, thereby substantially reducing the number of mRNA transcripts to be translated into a polypeptide. A ribozyme having specificity for a nucleic acid sequence can be designed (see for example: Cech et al. U.S. Pat. No. 4,987,071; and Cech et al. U.S. Pat. No. 5,116,742). Alternatively, mRNA transcripts corresponding to a nucleic acid sequence can be used to select a catalytic RNA having a specific ribonuclease activity from a pool of RNA molecules (Bartel and Szostak (1993) Science 261, 1411-1418). The use of ribozymes for gene silencing in plants is known in the art (e.g., Atkins et al. (1994) WO 94/00012; Lenne et al. (1995) WO 95/03404; Lutziger et al. (2000) WO 00/00619; Prinsen et al. (1997) WO 97/13865 and Scott et al. (1997) WO 97/38116).

Gene silencing may also be achieved by insertion mutagenesis (for example, T-DNA insertion or transposon insertion) or by strategies as described by, among others, Angell and Baulcombe ((1999) Plant J 20(3): 357-62), (Amplicon VIGS WO 98/36083), or Baulcombe (WO 99/15682).

Gene silencing may also occur if there is a mutation on an endogenous gene and/or a mutation on an isolated gene/nucleic acid subsequently introduced into a plant. The reduction or substantial elimination may be caused by a non-functional polypeptide. For example, the polypeptide may bind to various interacting proteins; one or more mutation(s) and/or truncation(s) may therefore provide for a polypeptide that is still able to bind interacting proteins (such as receptor proteins) but that cannot exhibit its normal function (such as signalling ligand).

A further approach to gene silencing is by targeting nucleic acid sequences complementary to the regulatory region of the gene (e.g., the promoter and/or enhancers) to form triple helical structures that prevent transcription of the gene in target cells. See Helene, C., Anticancer Drug Res. 6, 569-84, 1991; Helene et al., Ann. N.Y. Acad. Sci. 660, 27-36 1992; and Maher, L.J. Bioassays 14, 807-15, 1992.

Other methods, such as the use of antibodies directed to an endogenous polypeptide for inhibiting its function in planta, or interference in the signalling pathway in which a polypeptide is involved, will be well known to the skilled man. In particular, it can be envisaged that manmade molecules may be useful for inhibiting the biological function of a target polypeptide, or for interfering with the signalling pathway in which the target polypeptide is involved.

Alternatively, a screening program may be set up to identify in a plant population natural variants of a gene, which variants encode polypeptides with reduced activity. Such natural variants may also be used for example, to perform homologous recombination.

Artificial and/or natural microRNAs (miRNAs) may be used to knock out gene expression and/or mRNA translation. Endogenous miRNAs are single stranded small RNAs of typically 19-24 nucleotides long. They function primarily to regulate gene expression and/or mRNA translation. Most plant microRNAs (miRNAs) have perfect or near-perfect complementarity with their target sequences. However, there are natural targets with up to five mismatches. They are processed from longer non-coding RNAs with characteristic fold-back structures by double-strand specific RNases of the Dicer family. Upon processing, they are incorporated in the RNA-induced silencing complex (RISC) by binding to its main component, an Argonaute protein. MiRNAs serve as the specificity components of RISC, since they base-pair to target nucleic acids, mostly mRNAs, in the cytoplasm. Subsequent regulatory events include target mRNA cleavage and destruction and/or translational inhibition. Effects of miRNA overexpression are thus often reflected in decreased mRNA levels of target genes.

Artificial microRNAs (amiRNAs), which are typically 21 nucleotides in length, can be genetically engineered specifically to negatively regulate gene expression of single or multiple genes of interest. Determinants of plant microRNA target selection are well known in the art. Empirical parameters for target recognition have been defined and can be used to aid in the design of specific amiRNAs, (Schwab et al., Dev. Cell 8, 517-527, 2005). Convenient tools for design and generation of amiRNAs and their precursors are also available to the public (Schwab et al., Plant Cell 18, 1121-1133, 2006).

For optimal performance, the gene silencing techniques used for reducing expression in a plant of an endogenous gene requires the use of nucleic acid sequences from monocotyledonous plants for transformation of monocotyledonous plants, and from dicotyledonous plants for transformation of dicotyledonous plants. Preferably, a nucleic acid sequence from any given plant species is introduced into that same species. For example, a nucleic acid sequence from rice is transformed into a rice plant. However, it is not an absolute requirement that the nucleic acid sequence to be introduced originates from the same plant species as the plant in which it will be introduced. It is sufficient that there is substantial homology between the endogenous target gene and the nucleic acid to be introduced.

Described above are examples of various methods for the reduction or substantial elimination of expression in a plant of an endogenous gene. A person skilled in the art would readily be able to adapt the aforementioned methods for silencing so as to achieve reduction of expression of an endogenous gene in a whole plant or in parts thereof through the use of an appropriate promoter, for example.

Selectable Marker (Gene)/Reporter Gene

“Selectable marker”, “selectable marker gene” or “reporter gene” includes any gene that confers a phenotype on a cell in which it is expressed to facilitate the identification and/or selection of cells that are transfected or transformed with a nucleic acid construct of the invention. These marker genes enable the identification of a successful transfer of the nucleic acid molecules via a series of different principles. Suitable markers may be selected from markers that confer antibiotic or herbicide resistance, that introduce a new metabolic trait or that allow visual selection. Examples of selectable marker genes include genes conferring resistance to antibiotics (such as nptII that phosphorylates neomycin and kanamycin, or hpt, phosphorylating hygromycin, or genes conferring resistance to, for example, bleomycin, streptomycin, tetracyclin, chloramphenicol, ampicillin, gentamycin, geneticin (G418), spectinomycin or blasticidin), to herbicides (for example bar which provides resistance to Basta®; aroA or gox providing resistance against glyphosate, or the genes conferring resistance to, for example, imidazolinone, phosphinothricin or sulfonylurea), or genes that provide a metabolic trait (such as manA that allows plants to use mannose as sole carbon source or xylose isomerase for the utilisation of xylose, or antinutritive markers such as the resistance to 2-deoxyglucose). Expression of visual marker genes results in the formation of colour (for example β-glucuronidase, GUS or β-galactosidase with its coloured substrates, for example X-Gal), luminescence (such as the luciferin/luceferase system) or fluorescence (Green Fluorescent Protein, GFP, and derivatives thereof). This list represents only a small number of possible markers. The skilled worker is familiar with such markers. Different markers are preferred, depending on the organism and the selection method.

It is known that upon stable or transient integration of nucleic acids into plant cells, only a minority of the cells takes up the foreign DNA and, if desired, integrates it into its genome, depending on the expression vector used and the transfection technique used. To identify and select these integrants, a gene coding for a selectable marker (such as the ones described above) is usually introduced into the host cells together with the gene of interest. These markers can for example be used in mutants in which these genes are not functional by, for example, deletion by conventional methods. Furthermore, nucleic acid molecules encoding a selectable marker can be introduced into a host cell on the same vector that comprises the sequence encoding the polypeptides of the invention or used in the methods of the invention, or else in a separate vector. Cells which have been stably transfected with the introduced nucleic acid can be identified for example by selection (for example, cells which have integrated the selectable marker survive whereas the other cells die).

Since the marker genes, particularly genes for resistance to antibiotics and herbicides, are no longer required or are undesired in the transgenic host cell once the nucleic acids have been introduced successfully, the process according to the invention for introducing the nucleic acids advantageously employs techniques which enable the removal or excision of these marker genes. One such a method is what is known as co-transformation. The co-transformation method employs two vectors simultaneously for the transformation, one vector bearing the nucleic acid according to the invention and a second bearing the marker gene(s). A large proportion of transformants receives or, in the case of plants, comprises (up to 40% or more of the transformants), both vectors. In case of transformation with Agrobacteria, the transformants usually receive only a part of the vector, i.e. the sequence flanked by the T-DNA, which usually represents the expression cassette. The marker genes can subsequently be removed from the transformed plant by performing crosses. In another method, marker genes integrated into a transposon are used for the transformation together with desired nucleic acid (known as the Ac/Ds technology). The transformants can be crossed with a transposase source or the transformants are transformed with a nucleic acid construct conferring expression of a transposase, transiently or stable. In some cases (approx. 10%), the transposon jumps out of the genome of the host cell once transformation has taken place successfully and is lost. In a further number of cases, the transposon jumps to a different location. In these cases the marker gene must be eliminated by performing crosses. In microbiology, techniques were developed which make possible, or facilitate, the detection of such events. A further advantageous method relies on what is known as recombination systems; whose advantage is that elimination by crossing can be dispensed with. The best-known system of this type is what is known as the Cre/lox system. Cre1 is a recombinase that removes the sequences located between the loxP sequences. If the marker gene is integrated between the loxP sequences, it is removed once transformation has taken place successfully, by expression of the recombinase. Further recombination systems are the HIN/HIX, FLP/FRT and REP/STB system (Tribble et al., J. Biol. Chem., 275, 2000: 22255-22267; Velmurugan et al., J. Cell Biol., 149, 2000: 553-566). A site-specific integration into the plant genome of the nucleic acid sequences according to the invention is possible. Naturally, these methods can also be applied to microorganisms such as yeast, fungi or bacteria.

Transgenic/Transgene/Recombinant

For the purposes of the invention, “transgenic”, “transgene” or “recombinant” means with regard to, for example, a nucleic acid sequence, an expression cassette, gene construct or a vector comprising the nucleic acid sequence or an organism transformed with the nucleic acid sequences, expression cassettes or vectors according to the invention, all those constructions brought about by recombinant methods in which either

-   (a) the nucleic acid sequences encoding proteins useful in the     methods of the invention, or -   (b) genetic control sequence(s) which is operably linked with the     nucleic acid sequence according to the invention, for example a     promoter, or -   (c) a) and b)     are not located in their natural genetic environment or have been     modified by recombinant methods, it being possible for the     modification to take the form of, for example, a substitution,     addition, deletion, inversion or insertion of one or more nucleotide     residues. The natural genetic environment is understood as meaning     the natural genomic or chromosomal locus in the original plant or     the presence in a genomic library. In the case of a genomic library,     the natural genetic environment of the nucleic acid sequence is     preferably retained, at least in part. The environment flanks the     nucleic acid sequence at least on one side and has a sequence length     of at least 50 bp, preferably at least 500 bp, especially preferably     at least 1000 bp, most preferably at least 5000 bp. A naturally     occurring expression cassette—for example the naturally occurring     combination of the natural promoter of the nucleic acid sequences     with the corresponding nucleic acid sequence encoding a polypeptide     useful in the methods of the present invention, as defined     above—becomes a transgenic expression cassette when this expression     cassette is modified by non-natural, synthetic (“artificial”)     methods such as, for example, mutagenic treatment. Suitable methods     are described, for example, in U.S. Pat. No. 5,565,350 or WO     00/15815.

A transgenic plant for the purposes of the invention is thus understood as meaning, as above, that the nucleic acids used in the method of the invention are not at their natural locus in the genome of said plant, it being possible for the nucleic acids to be expressed homologously or heterologously. However, as mentioned, transgenic also means that, while the nucleic acids according to the invention or used in the inventive method are at their natural position in the genome of a plant, the sequence has been modified with regard to the natural sequence, and/or that the regulatory sequences of the natural sequences have been modified. Transgenic is preferably understood as meaning the expression of the nucleic acids according to the invention at an unnatural locus in the genome, i.e. homologous or, preferably, heterologous expression of the nucleic acids takes place. Preferred transgenic plants are mentioned herein.

Transformation

The term “introduction” or “transformation” as referred to herein encompasses the transfer of an exogenous polynucleotide into a host cell, irrespective of the method used for transfer. Plant tissue capable of subsequent clonal propagation, whether by organogenesis or embryogenesis, may be transformed with a genetic construct of the present invention and a whole plant regenerated there from. The particular tissue chosen will vary depending on the clonal propagation systems available for, and best suited to, the particular species being transformed. Exemplary tissue targets include leaf disks, pollen, embryos, cotyledons, hypocotyls, megagametophytes, callus tissue, existing meristematic tissue (e.g., apical meristem, axillary buds, and root meristems), and induced meristem tissue (e.g., cotyledon meristem and hypocotyl meristem). The polynucleotide may be transiently or stably introduced into a host cell and may be maintained non-integrated, for example, as a plasmid. Alternatively, it may be integrated into the host genome. The resulting transformed plant cell may then be used to regenerate a transformed plant in a manner known to persons skilled in the art.

The transfer of foreign genes into the genome of a plant is called transformation. Transformation of plant species is now a fairly routine technique. Advantageously, any of several transformation methods may be used to introduce the gene of interest into a suitable ancestor cell. The methods described for the transformation and regeneration of plants from plant tissues or plant cells may be utilized for transient or for stable transformation. Transformation methods include the use of liposomes, electroporation, chemicals that increase free DNA uptake, injection of the DNA directly into the plant, particle gun bombardment, transformation using viruses or pollen and microprojection. Methods may be selected from the calcium/polyethylene glycol method for protoplasts (Krens, F. A. et al., (1982) Nature 296, 72-74; Negrutiu I et al. (1987) Plant Mol Biol 8: 363-373); electroporation of protoplasts (Shillito R. D. et al. (1985) Bio/Technol 3, 1099-1102); microinjection into plant material (Crossway A et al., (1986) Mol. Gen Genet 202: 179-185); DNA or RNA-coated particle bombardment (Klein T M et al., (1987) Nature 327: 70) infection with (non-integrative) viruses and the like. Transgenic plants, including transgenic crop plants, are preferably produced via Agrobacterium-mediated transformation. An advantageous transformation method is the transformation in planta. To this end, it is possible, for example, to allow the agrobacteria to act on plant seeds or to inoculate the plant meristem with agrobacteria. It has proved particularly expedient in accordance with the invention to allow a suspension of transformed agrobacteria to act on the intact plant or at least on the flower primordia. The plant is subsequently grown on until the seeds of the treated plant are obtained (Clough and Bent, Plant J. (1998) 16, 735-743). Methods for Agrobacterium-mediated transformation of rice include well known methods for rice transformation, such as those described in any of the following: European patent application EP 1198985 A1, Aldemita and Hodges (Planta 199: 612-617, 1996); Chan et al. (Plant Mol Biol 22 (3): 491-506, 1993), Hiei et al. (Plant J 6 (2): 271-282, 1994), which disclosures are incorporated by reference herein as if fully set forth. In the case of corn transformation, the preferred method is as described in either Ishida et al. (Nat. Biotechnol 14(6): 745-50, 1996) or Frame et al. (Plant Physiol 129(1): 13-22, 2002), which disclosures are incorporated by reference herein as if fully set forth. Said methods are further described by way of example in B. Jenes et al., Techniques for Gene Transfer, in: Transgenic Plants, Vol. 1, Engineering and Utilization, eds. S. D. Kung and R. Wu, Academic Press (1993) 128-143 and in Potrykus Annu. Rev. Plant Physiol. Plant Molec. Biol. 42 (1991) 205-225). The nucleic acids or the construct to be expressed is preferably cloned into a vector, which is suitable for transforming Agrobacterium tumefaciens, for example pBin19 (Bevan et al., Nucl. Acids Res. 12 (1984) 8711). Agrobacteria transformed by such a vector can then be used in known manner for the transformation of plants, such as plants used as a model, like Arabidopsis (Arabidopsis thaliana is within the scope of the present invention not considered as a crop plant), or crop plants such as, by way of example, tobacco plants, for example by immersing bruised leaves or chopped leaves in an agrobacterial solution and then culturing them in suitable media. The transformation of plants by means of Agrobacterium tumefaciens is described, for example, by Höfgen and Willmitzer in Nucl. Acid Res. (1988) 16, 9877 or is known inter alia from F. F. White, Vectors for Gene Transfer in Higher Plants; in Transgenic Plants, Vol. 1, Engineering and Utilization, eds. S. D. Kung and R. Wu, Academic Press, 1993, pp. 15-38.

In addition to the transformation of somatic cells, which then have to be regenerated into intact plants, it is also possible to transform the cells of plant meristems and in particular those cells which develop into gametes. In this case, the transformed gametes follow the natural plant development, giving rise to transgenic plants. Thus, for example, seeds of Arabidopsis are treated with Agrobacteria and seeds are obtained from the developing plants of which a certain proportion is transformed and thus transgenic [Feldman, K A and Marks M D (1987). Mol Gen Genet 208:274-289; Feldmann K (1992). In: C Koncz, N-H Chua and J Shell, eds, Methods in Arabidopsis Research. Word Scientific, Singapore, pp. 274-289]. Alternative methods are based on the repeated removal of the inflorescences and incubation of the excision site in the center of the rosette with transformed agrobacteria, whereby transformed seeds can likewise be obtained at a later point in time (Chang (1994). Plant J. 5: 551-558; Katavic (1994). Mol Gen Genet, 245: 363-370). However, an especially effective method is the vacuum infiltration method with its modifications such as the “floral dip” method. In the case of vacuum infiltration of Arabidopsis, intact plants under reduced pressure are treated with an agrobacterial suspension [Bechthold, N (1993). C R Acad Sci Paris Life Sci, 316: 1194-1199], while in the case of the “floral dip” method the developing floral tissue is incubated briefly with a surfactant-treated agrobacterial suspension [Clough, S J and Bent A F (1998) The Plant J. 16, 735-743]. A certain proportion of transgenic seeds are harvested in both cases, and these seeds can be distinguished from non-transgenic seeds by growing under the above-described selective conditions. In addition the stable transformation of plastids is of advantages because plastids are inherited maternally is most crops reducing or eliminating the risk of transgene flow through pollen. The transformation of the chloroplast genome is generally achieved by a process which has been schematically displayed in Klaus et al., 2004 [Nature Biotechnology 22 (2), 225-229]. Briefly the sequences to be transformed are cloned together with a selectable marker gene between flanking sequences homologous to the chloroplast genome. These homologous flanking sequences direct site specific integration into the plastome. Plastidal transformation has been described for many different plant species and an overview is given in Bock (2001) Transgenic plastids in basic research and plant biotechnology. J Mol Biol. 2001 Sep. 21; 312 (3):425-38 or Maliga, P (2003) Progress towards commercialization of plastid transformation technology. Trends Biotechnol. 21, 20-28. Further biotechnological progress has recently been reported in form of marker free plastid transformants, which can be produced by a transient co-integrated maker gene (Klaus et al., 2004, Nature Biotechnology 22(2), 225-229).

T-DNA Activation Tagging

T-DNA activation tagging (Hayashi et al. Science (1992) 1350-1353), involves insertion of T-DNA, usually containing a promoter (may also be a translation enhancer or an intron), in the genomic region of the gene of interest or 10 kb up- or downstream of the coding region of a gene in a configuration such that the promoter directs expression of the targeted gene. Typically, regulation of expression of the targeted gene by its natural promoter is disrupted and the gene falls under the control of the newly introduced promoter. The promoter is typically embedded in a T-DNA. This T-DNA is randomly inserted into the plant genome, for example, through Agrobacterium infection and leads to modified expression of genes near the inserted T-DNA. The resulting transgenic plants show dominant phenotypes due to modified expression of genes close to the introduced promoter.

TILLING

The term “TILLING” is an abbreviation of “Targeted Induced Local Lesions In Genomes” and refers to a mutagenesis technology useful to generate and/or identify nucleic acids encoding proteins with modified expression and/or activity. TILLING also allows selection of plants carrying such mutant variants. These mutant variants may exhibit modified expression, either in strength or in location or in timing (if the mutations affect the promoter for example). These mutant variants may exhibit higher activity than that exhibited by the gene in its natural form. TILLING combines high-density mutagenesis with high-throughput screening methods. The steps typically followed in TILLING are: (a) EMS mutagenesis (Redei G P and Koncz C (1992) In Methods in Arabidopsis Research, Koncz C, Chua N H, Schell J, eds. Singapore, World Scientific Publishing Co, pp. 16-82; Feldmann et al., (1994) In Meyerowitz E M, Somerville C R, eds, Arabidopsis. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., pp 137-172; Lightner J and Caspar T (1998) In J Martinez-Zapater, J Salinas, eds, Methods on Molecular Biology, Vol. 82. Humana Press, Totowa, N.J., pp 91-104); (b) DNA preparation and pooling of individuals; (c) PCR amplification of a region of interest; (d) denaturation and annealing to allow formation of heteroduplexes; (e) DHPLC, where the presence of a heteroduplex in a pool is detected as an extra peak in the chromatogram; (f) identification of the mutant individual; and (g) sequencing of the mutant PCR product. Methods for TILLING are well known in the art (McCallum et al., (2000) Nat Biotechnol 18: 455-457; reviewed by Stemple (2004) Nat Rev Genet 5(2): 145-50).

Homologous Recombination

Homologous recombination allows introduction in a genome of a selected nucleic acid at a defined selected position. Homologous recombination is a standard technology used routinely in biological sciences for lower organisms such as yeast or the moss Physcomitrella. Methods for performing homologous recombination in plants have been described not only for model plants (Offringa et al. (1990) EMBO J 9(10): 3077-84) but also for crop plants, for example rice (Terada et al. (2002) Nat Biotech 20(10): 1030-4; lida and Terada (2004) Curr Opin Biotech 15(2): 132-8), and approaches exist that are generally applicable regardless of the target organism (Miller et al, Nature Biotechnol. 25, 778-785, 2007).

Increase/Improve/Enhance

The terms “increase”, “improve” or “enhance” are interchangeable and shall mean in the sense of the application at least a 3%, 4%, 5%, 6%, 7%, 8%, 9% or 10%, preferably at least 15% or 20%, more preferably 25%, 30%, 35% or 40% more of the factor in question in comparison to any control.

Plant

The term “plant” as used herein encompasses whole plants, ancestors and progeny of the plants and plant parts, including seeds, shoots, stems, leaves, roots (including tubers), flowers, and tissues and organs, wherein each of the aforementioned comprise the gene/nucleic acid of interest. The term “plant” also encompasses plant cells, suspension cultures, callus tissue, embryos, meristematic regions, gametophytes, sporophytes, pollen and microspores, again wherein each of the aforementioned comprises the gene/nucleic acid of interest.

Plants that are particularly useful in the methods of the invention include all plants which belong to the superfamily Viridiplantae, in particular monocotyledonous and dicotyledonous plants including fodder or forage legumes, ornamental plants, food crops, trees or shrubs selected from the list comprising Acer spp., Actinidia spp., Abelmoschus spp., Agave sisalana, Agropyron spp., Agrostis stolonifera, Allium spp., Amaranthus spp., Ammophila arenaria, Ananas comosus, Annona spp., Apium graveolens, Arachis spp, Artocarpus spp., Asparagus officinalis, Avena spp. (e.g. Avena sativa, Avena fatua, Avena byzantina, Avena fatua var. sativa, Avena hybrida), Averrhoa carambola, Bambusa sp., Benincasa hispida, Bertholletia excelsea, Beta vulgaris, Brassica spp. (e.g. Brassica napus, Brassica rapa ssp. [canola, oilseed rape, turnip rape]), Cadaba farinosa, Camellia sinensis, Canna indica, Cannabis sativa, Capsicum spp., Carex elata, Carica papaya, Carissa macrocarpa, Carya spp., Carthamus tinctorius, Castanea spp., Ceiba pentandra, Cichorium endivia, Cinnamomum spp., Citrullus lanatus, Citrus spp., Cocos spp., Coffea spp., Colocasia esculenta, Cola spp., Corchorus sp., Coriandrum sativum, Corylus spp., Crataegus spp., Crocus sativus, Cucurbita spp., Cucumis spp., Cynara spp., Daucus carota, Desmodium spp., Dimocarpus longan, Dioscorea spp., Diospyros spp., Echinochloa spp., Elaeis (e.g. Elaeis guineensis, Elaeis oleifera), Eleusine coracana, Erianthus sp., Eriobotrya japonica, Eucalyptus sp., Eugenia uniflora, Fagopyrum spp., Fagus spp., Festuca arundinacea, Ficus carica, Fortunella spp., Fragaria spp., Ginkgo biloba, Glycine spp. (e.g. Glycine max, Soja hispida or Soja max), Gossypium hirsutum, Helianthus spp. (e.g. Helianthus annuus), Hemerocallis fulva, Hibiscus spp., Hordeum spp. (e.g. Hordeum vulgare), Ipomoea batatas, Juglans spp., Lactuca sativa, Lathyrus spp., Lens culinaris, Linum usitatissimum, Litchi chinensis, Lotus spp., Luffa acutangula, Lupinus spp., Luzula sylvatica, Lycopersicon spp. (e.g. Lycopersicon esculentum, Lycopersicon lycopersicum, Lycopersicon pyriforme), Macrotyloma spp., Malus spp., Malpighia emarginata, Mammea americana, Mangifera indica, Manihot spp., Manilkara zapota, Medicago sativa, Melilotus spp., Mentha spp., Miscanthus sinensis, Momordica spp., Morus nigra, Musa spp., Nicotiana spp., Olea spp., Opuntia spp., Ornithopus spp., Oryza spp. (e.g. Oryza sativa, Oryza latifolia), Panicum miliaceum, Panicum virgatum, Passiflora edulis, Pastinaca sativa, Pennisetum sp., Persea spp., Petroselinum crispum, Phalaris arundinacea, Phaseolus spp., Phleum pratense, Phoenix spp., Phragmites australis, Physalis spp., Pinus spp., Pistacia vera, Pisum spp., Poa spp., Populus spp., Prosopis spp., Prunus spp., Psidium spp., Punica granatum, Pyrus communis, Quercus spp., Raphanus sativus, Rheum rhabarbarum, Ribes spp., Ricinus communis, Rubus spp., Saccharum spp., Salix sp., Sambucus spp., Secale cereale, Sesamum spp., Sinapis sp., Solanum spp. (e.g. Solanum tuberosum, Solanum integrifolium or Solanum lycopersicum), Sorghum bicolor, Spinacia spp., Syzygium spp., Tagetes spp., Tamarindus indica, Theobroma cacao, Trifolium spp., Triticosecale rimpaui, Triticum spp. (e.g. Triticum aestivum, Triticum durum, Triticum turgidum, Triticum hybernum, Triticum macha, Triticum sativum or Triticum vulgare), Tropaeolum minus, Tropaeolum majus, Vaccinium spp., Vicia spp., Vigna spp., Viola odorata, Vitis spp., Zea mays, Zizania palustris, Ziziphus spp., amongst others.

DETAILED DESCRIPTION OF THE INVENTION

Surprisingly, it has now been found that modulating expression in a plant of a nucleic acid encoding a UBP15 polypeptide or a homologue thereof gives plants having altered growth and/or development relative to control plants. According to a first embodiment, the present invention provides a method for altering plant growth and/or development relative to control plants, comprising modulating expression in a plant of a nucleic acid encoding a UBP15 polypeptide or a homologue thereof.

A preferred method for modulating (preferably, increasing) expression of a nucleic acid encoding a UBP15 polypeptide or a homologue thereof is by introducing and expressing in a plant a nucleic acid encoding a UBP15 polypeptide or a homologue thereof.

Any reference hereinafter to a “protein useful in the methods of the invention” is taken to mean a UBP polypeptide of the UBP15 subfamily or a homologue thereof as defined herein. Any reference hereinafter to a “nucleic acid useful in the methods of the invention” is taken to mean a nucleic acid capable of encoding such a UBP polypeptide. The nucleic acid to be introduced into a plant (and therefore useful in performing the methods of the invention) is any nucleic acid encoding the type of protein which will now be described, hereinafter also referred to as “UBP15 nucleic acid” or “UBP15 gene”.

A “UBP15 polypeptide” as defined herein refers to any polypeptide comprising each of the following:

-   -   (i) a Cysteine box (Cys box); and     -   (ii) a Histidine box (His box); and     -   (iii) a ZnMYND zinc finger domain.

The Cys and His box are two well conserved motifs found in a conserved catalytic domain called the UBP domain (see FIG. 1). The Cys box and the His box comprise the catalytic triad residues (Cys in Cys box, His and Asp/Asn in His box) (Amerik and Hochstrasser, 2004). The length of UBP domains vary from 300 to 900 amino acids in length, and despite sometimes having low overall sequence conservation, they typically display a conserved three dimensional structure. Within the UBP domains, the Cysteine in Cys box plays an essential role in catalytic activity and specific mutation in the Cysteine can abolish the de-ubiquitination activity of UBPs (Papa and Hochstrasser, 1993; Chandler et al., 1997; Rao-Naik et al., 2000; Yan et al., 2000; Baek et al., 2001; Doelling et al., 2001; Hanna et al., 2006).

The UBP15 subfamily includes UBP15, UBP16, UBP17, UBP18 and UBP19. Members of this subfamily and homologues thereof comprise a signature MYND type Zinc finger domain, which was reported to be a protein-protein interaction domain in mammals (Gross and McGinnis, 1996; Lutterbach et al., 1998a; Lutterbach et al., 1998b; Masselink and Bernards, 2000).

A genetic interaction analysis among members of the UBP15 subfamily revealed that UBP15 and UBP16, but not UBP17, have functional redundancy, even though UBP16 and UBP17 are equally related to UBP15. Mutation of another subfamily member, UBP19, leads to embryo lethality, while loss-of-function of its closest related member, UBP18, exhibits no visible defect.

UBP sequences useful in performing the methods of the invention may also be identified by including a query sequence in a UBP phylogenetic tree, such as the one depicted in FIG. 1. UBP15 polypeptides or homologues thereof will cluster with the UPB15 subfamily rather than with any other subfamily.

Furthermore, UBP15 polypeptides and homologues thereof typically have UBP activity In vitro.

UBP15 polypeptides or homologues thereof useful in the methods of the invention typically have in increasing order of preference at least 50%, 51%, 52%, 53%, 54%, 55%, 56%, 57%, 58%, 59%, 60%, 61%, 62%, 63%, 64%, 65%, 66%, 67%, 68%, 69%, 70%, 71%, 72%, 73%, 74%, 75%, 76%, 77%, 78%, 79%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% overall sequence identity to any one of UBP15 (SEQ ID NO: 2), UBP16 (SEQ ID NO: 4), UBP17 (SEQ ID NO: 6), UBP18 (SEQ ID NO: 8) or UBP19 (SEQ ID NO: 10) from Arabidopsis thaliana. The overall sequence identity may be determined using a global alignment algorithm, such as the Needleman Wunsch algorithm in the program GAP (GCG Wisconsin Package, Accelrys), preferably with default parameters. Compared to overall sequence identity, the sequence identity will generally be higher when only conserved domains or motifs are considered.

The term “domain” and “motif” is defined in the “definitions” section herein. Specialist databases exist for the identification of domains, for example, SMART (Schultz et al. (1998) Proc. Natl. Acad. Sci. USA 95, 5857-5864; Letunic et al. (2002) Nucleic Acids Res 30, 242-244), InterPro (Mulder et al., (2003) Nucl. Acids. Res. 31, 315-318), Prosite (Bucher and Bairoch (1994), A generalized profile syntax for biomolecular sequences motifs and its function in automatic sequence interpretation. (In) ISMB-94; Proceedings 2nd International Conference on Intelligent Systems for Molecular Biology. Altman R., Brutlag D., Karp P., Lathrop R., Searls D., Eds., pp 53-61, AAAI Press, Menlo Park; Hulo et al., Nucl. Acids. Res. 32:D134-D137, (2004)), or Pfam (Bateman et al., Nucleic Acids Research 30(1): 276-280 (2002)). A set of tools for in silico analysis of protein sequences is available on the ExPASy proteomics server (Swiss Institute of Bioinformatics (Gasteiger et al., ExPASy: the proteomics server for in-depth protein knowledge and analysis, Nucleic Acids Res. 31:3784-3788(2003)). Domains or motifs may also be identified using routine techniques, such as by sequence alignment.

Methods for the alignment of sequences for comparison are well known in the art, such methods include GAP, BESTFIT, BLAST, FASTA and TFASTA. GAP uses the algorithm of Needleman and Wunsch ((1970) J Mol Biol 48: 443-453) to find the global (i.e. spanning the complete sequences) alignment of two sequences that maximizes the number of matches and minimizes the number of gaps. The BLAST algorithm (Altschul et al. (1990) J Mol Biol 215: 403-10) calculates percent sequence identity and performs a statistical analysis of the similarity between the two sequences. The software for performing BLAST analysis is publicly available through the National Centre for Biotechnology Information (NCBI). Homologues may readily be identified using, for example, the ClustalW multiple sequence alignment algorithm (version 1.83), with the default pairwise alignment parameters, and a scoring method in percentage. Global percentages of similarity and identity may also be determined using one of the methods available in the MatGAT software package (Campanella et al., BMC Bioinformatics. 2003 Jul. 10;4:29. MatGAT: an application that generates similarity/identity matrices using protein or DNA sequences.). Minor manual editing may be performed to optimise alignment between conserved motifs, as would be apparent to a person skilled in the art. Furthermore, instead of using full-length sequences for the identification of homologues, specific domains may also be used. The sequence identity values may be determined over the entire nucleic acid or amino acid sequence or over selected domains or conserved motif(s), using the programs mentioned above using the default parameters. For local alignments, the Smith-Waterman algorithm is particularly useful (Smith T F, Waterman M S (1981) J. Mol. Biol 147(1); 195-7).

Examples of nucleic acids encoding members of the UBP15 subfamily are represented by SEQ ID NOs 1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 39 and 44. Such nucleic acids are useful in performing the methods of the invention. The nucleotide sequence represented by SEQ ID NO: 11 encodes the polypeptide sequence represented by SEQ ID NO: 12, a UBP from rice (Nipponbare strain) that is closely related to AtUBP15, and has 53% identity to AtUBP15 on a nucleotide level, 40% identity on a protein level and 54% similarity on a protein level. The nucleotide sequence represented by SEQ ID NO: 13 encodes the polypeptide sequence represented by SEQ ID NO: 14, a UBP from rice (Nipponbare strain) that is closely related to AtUBP16, and has 44% identity to AtUBP16 on a nucleotide level, 30% identity on a protein level and 44% similarity on a protein level to AtUBP16. The nucleotide sequence represented by SEQ ID NO: 15 encodes the polypeptide sequence represented by SEQ ID NO: 16, a UBP from rice (Nipponbare strain) that is closely related to AtUBP17, and has 40% identity to AtUBP17 on a nucleotide level, 33% identity on a protein level and 45% similarity on a protein level to AtUBP17. The nucleotide sequence represented by SEQ ID NO: 17 encodes the polypeptide sequence represented by SEQ ID NO: 18, a UBP from rice (Nipponbare strain) that is closely related to AtUBP18, and has 34% identity to AtUBP17 on a nucleotide level, 30% identity on a protein level and 39% similarity on a protein level to AtUBP18. SEQ ID NO: 19 is a nucleotide sequence from maize (Zea mays) showing some similarity to SEQ ID NO: 11. SEQ ID NO: 19 is the longest cDNA sequence of maize obtained by assembling the ESTs of SEQ ID NOs 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37 and 38. SEQ ID NO: 39 is another nucleotide sequence from maize showing some similarity to SEQ ID NO: 11. SEQ ID NO: 39 was assembled from the ESTs of SEQ ID NOs 40, 41, 42 and 43. SEQ ID NO: 44 is another nucleotide sequence from maize showing some similarity to SEQ ID NO: 11. SEQ ID NO: 44 was assembled from the ESTs of SEQ ID NOs 45, 46, 47, 48, 49, 50 and 51.

SEQ ID NOs 12, 14, 16 and 18 are examples of orthologues of the UBP polypeptides represented by SEQ ID NOs: 2, 4, 6 and 8, respectively. The terms “orthologues” and “paralogues” are as defined herein. Further orthologues and paralogues may readily be identified by performing a so-called reciprocal blast search. Typically, this involves a first BLAST involving BLASTing a query sequence (for example using any of sequences SEQ ID NOs 2, 4, 6, 8 or 10) against any sequence database, such as the publicly available NCBI database. BLASTN or TBLASTX (using standard default values) are generally used when starting from a nucleotide sequence, and BLASTP or TBLASTN (using standard default values) when starting from a protein sequence. The BLAST results may optionally be filtered. The full-length sequences of either the filtered results or non-filtered results are then BLASTed back (second BLAST) against sequences from the organism from which the query sequence is derived (where the query sequence is SEQ ID NO: 1 to SEQ ID NO: 10, the second BLAST would therefore be against Arabidopsis sequences). The results of the first and second BLASTs are then compared. A paralogue is identified if a high-ranking hit from the first blast is from the same species as from which the query sequence is derived, a BLAST back then ideally results in the query sequence being amongst the highest hits; an orthologue is identified if a high-ranking hit in the first BLAST is not from the same species as from which the query sequence is derived, and preferably results upon BLAST back in the query sequence being among the highest hits.

High-ranking hits are those having a low E-value. The lower the E-value, the more significant the score (or in other words the lower the chance that the hit was found by chance). Computation of the E-value is well known in the art. In addition to E-values, comparisons are also scored by percentage identity. Percentage identity refers to the number of identical nucleotides (or amino acids) between the two compared nucleic acid (or polypeptide) sequences over a particular length. In the case of large families, ClustalW may be used, followed by a neighbour joining tree, to help visualize clustering of related genes and to identify orthologues and paralogues.

Nucleic acid variants may also be useful in practising the methods of the invention. Examples of such variants include nucleic acids encoding homologues and derivatives of any one of the amino acid sequences represented by SEQ ID NOs 2, 4, 6, 8 or 10, the terms “homologue” and “derivative” being as defined herein. Also useful in the methods of the invention are nucleic acids encoding homologues and derivatives of orthologues or paralogues of any one of the amino acid sequences represented by SEQ ID NOs 2, 4, 6, 8 or 10. Homologues and derivatives useful in the methods of the present invention have substantially the same biological and functional activity as the unmodified protein from which they are derived.

Further nucleic acid variants useful in practising the methods of the invention include portions of nucleic acids encoding UBP15 polypeptides or homologues thereof, nucleic acids hybridising to nucleic acids encoding UBP15 polypeptides or homologues thereof, splice variants of nucleic acids encoding UBP15 polypeptides or homologues thereof, allelic variants of nucleic acids encoding UBP15 polypeptides or homologues thereof and variants of nucleic acids encoding UBP15 polypeptides obtained by gene shuffling. The terms hybridising sequence, splice variant, allelic variant and gene shuffling are as described herein.

Nucleic acids encoding UBP15 polypeptides or homologues thereof need not be full-length nucleic acids, since performance of the methods of the invention does not rely on the use of full-length nucleic acid sequences. According to the present invention, there is provided a method for altering plant growth and development, comprising introducing and expressing in a plant a portion of any one of the nucleic acid sequences represented by SEQ ID NOs 1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 39 or 44, or a portion of a nucleic acid encoding an orthologue, paralogue or homologue of any of the amino acid sequences represented by SEQ ID NOs 2, 4, 6, 8, 10, 12, 14, 16 or 18.

A portion of a nucleic acid may be prepared, for example, by making one or more deletions to the nucleic acid. The portions may be used in isolated form or they may be fused to other coding (or non-coding) sequences in order to, for example, produce a protein that combines several activities. When fused to other coding sequences, the resultant polypeptide produced upon translation may be bigger than that predicted for the protein portion.

Portions useful in the methods of the invention, encode a UBP15 polypeptide or a homologue thereof as defined herein, and have substantially the same biological activity as the amino acid sequences represented by any of SEQ ID NOs 2, 4, 6, 8, 10, 12, 14, 16 or 18. Preferably, the portion is a portion of any one of the nucleic acids given in represented by SEQ ID NOs 1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 39 or 44, or is a portion of a nucleic acid encoding an orthologue or paralogue of any one of the amino acid sequences represented by SEQ ID NOs 2, 4, 6, 8, 10, 12, 14, 16 or 18. Preferably the portion is at least 1000, 1050, 1100, 1150, 1200, 1250, 1300, 1350, 1400, 1450, 1500, 1550, 1600, 1650, 1700, 1750, 1800, 1850, 1900, 1950, 2000, 2050, 2100, 2150, 1200, 2250, 2300, 2350, 2400, 2450, 2500, 2550, 2600, 2650, 2700, 2750, 2800, 2850, 2900, 2950, 3000, 3050, 3100, 3150 or more consecutive nucleotides in length, the consecutive nucleotides being of any one of the nucleic acid sequences represented by SEQ ID NOs 1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 39 or 44, or of a nucleic acid encoding an orthologue or paralogue of any one of the amino acid sequences represented by SEQ ID NOs 2, 4, 6, 8, 10, 12, 14, 16 or 18. Most preferably the portion is a portion of the nucleic acid of any one of SEQ ID NOs 1, 3, 5, 7 or 9. Preferably, the portion encodes a fragment of an amino acid sequence which, when used in the construction of a UBP phylogenetic tree, such as the one depicted in FIG. 1, clusters with the UBP15 subfamily of proteins rather than with any other subfamily of UBPs.

Another nucleic acid variant useful in the methods of the invention is a nucleic acid capable of hybridising, under reduced stringency conditions, preferably under stringent conditions, with a nucleic acid encoding a UBP15 polypeptide or a homologue thereof as defined herein, or with a portion as defined herein.

According to the present invention, there is provided a method for altering plant growth and/or development, comprising introducing and expressing in a plant a nucleic acid capable of hybridizing to any one of the nucleic acids represented by SEQ ID NOs 1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 39 or 44, or comprising introducing and expressing in a plant a nucleic acid capable of hybridising to a nucleic acid encoding an orthologue, paralogue or homologue of any of the nucleic acid sequences represented by SEQ ID NOs 2, 4, 6, 8, 10, 12, 14, 16 or, 18.

Hybridising sequences useful in the methods of the invention encode a UBP15 polypeptide as defined herein, having substantially the same biological activity as the amino acid sequences represented by any one of SEQ ID NOs 2, 4, 6, 8, 10, 12, 14, 16 or 18. Preferably, the hybridising sequence is capable of hybridising to any one of the nucleic acids represented by SEQ ID NOs 1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 39 or 44, or to a portion of any of these sequences, a portion being as defined above, or the hybridising sequence is capable of hybridising to a nucleic acid encoding an orthologue or paralogue of any one of the amino acid sequences represented by SEQ ID NOs 2, 4, 6, 8, 10, 12, 14, 16 or 18. Most preferably, the hybridising sequence is capable of hybridising to a nucleic acid as represented by SEQ ID NOs 1, 3, 5, 7, 9, 11, 13, 15 or 17 or to a portion thereof.

Preferably, the hybridising sequence encodes a polypeptide with an amino acid sequence which, when full-length and used in the construction of a UBP phylogenetic tree, such as the one depicted in FIG. 1, clusters with the subfamily of UBP15 polypeptides rather than with any other UBP subfamily.

Another nucleic acid variant useful in the methods of the invention is a splice variant encoding a UBP15 polypeptide or a homologue thereof as defined hereinabove, a splice variant being as defined herein.

According to the present invention, there is provided a method for altering plant growth and/or development, comprising introducing and expressing in a plant a splice variant of any one of the nucleic acid sequences represented by SEQ ID NOs 1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 39 or 44, or a splice variant of a nucleic acid encoding an orthologue, paralogue or homologue of any of the amino acid sequences represented by SEQ ID NOs 2, 4, 6, 8, 10, 12, 14, 16 or 18.

Preferred splice variants are splice variants of a nucleic acid represented by any one of SEQ ID NOs 1, 3, 5, 7, 9, 11, 13, 15 or 17, or a splice variant of a nucleic acid encoding an orthologue or paralogue of SEQ ID NO: 2, 4, 6, 8, 10, 12, 14, 16 or 18. Preferably, the amino acid sequence encoded by the splice variant, when used in the construction of a UBP phylogenetic tree, such as the one depicted in FIG. 1, clusters with the subfamily of UBP15 polypeptides rather than with any other UBP subfamily.

Another nucleic acid variant useful in performing the methods of the invention is an allelic variant of a nucleic acid encoding a UBP15 polypeptide or a homologue thereof as defined hereinabove, an allelic variant being as defined herein.

According to the present invention, there is provided a method for altering plant growth and/or development, comprising introducing and expressing in a plant an allelic variant of any one of the nucleic acids represented by SEQ ID NOs 1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 39 or 44, or comprising introducing and expressing in a plant an allelic variant of a nucleic acid encoding an orthologue, paralogue or homologue of any of the amino acid sequences represented by SEQ ID NOs 2, 4, 6, 8, 10, 12, 14, 16 or 18.

The allelic variants useful in the methods of the present invention have substantially the same biological activity as any one of the UBP15 subfamily polypeptides represented by SEQ ID NO: 2, 4, 6, 8, 10, 12, 14, 16 or 18. Allelic variants exist in nature, and encompassed within the methods of the present invention is the use of these natural alleles. Preferably, the allelic variant is an allelic variant of any one of SEQ ID NOs 1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 39 or 44, or an allelic variant of a nucleic acid encoding an orthologue or paralogue of SEQ ID NO: 2, 4, 6, 8, 10, 12, 14, 16 or 18. Preferably, the amino acid sequence encoded by the allelic variant, when used in the construction of a UBP phylogenetic tree, such as the one depicted in FIG. 1, clusters with the UBP15 subfamily rather than with any other UBP subfamily.

Gene shuffling or directed evolution may also be used to generate variants of nucleic acids encoding UBP15 polypeptides or homologues thereof as defined above; the term “gene shuffling” being as defined herein.

According to the present invention, there is provided a method for altering plant growth and/or development in plants, comprising introducing and expressing in a plant a variant of any one of the nucleic acid sequences represented by any one of SEQ ID NOs 1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 39 or 44, or comprising introducing and expressing in a plant a variant of a nucleic acid encoding an orthologue, paralogue or homologue of any of the amino acid sequences represented by any one of SEQ ID NOs 2, 4, 6, 8, 10, 12, 14, 16 or 18, which variant nucleic acid is obtained by gene shuffling.

Preferably, the amino acid sequence encoded by the variant nucleic acid obtained by gene shuffling, when used in the construction of a UBP phylogenetic tree such as the one depicted in FIG. 1, clusters with the subfamily of UBP15 polypeptides rather than with any other UBP subfamily.

Furthermore, nucleic acid variants may also be obtained by site-directed mutagenesis. Several methods are available to achieve site-directed mutagenesis, the most common being PCR based methods (Current Protocols in Molecular Biology. Wiley Eds.).

Nucleic acids encoding UBP15 polypeptides may be derived from any natural or artificial source. The nucleic acid may be modified from its native form in composition and/or genomic environment through deliberate human manipulation. Preferably the UBP polypeptide-encoding nucleic acid is from a plant, further preferably from a dicotyledonous plant, more preferably from the family Brassicaceae, most preferably the nucleic acid is from Arabidopsis thaliana.

Performance of the methods of the invention gives plants having altered plant growth and/or development.

The altered development may be in any part of a plant, in any cell, tissue or organ, particularly in the leaves. The altered development may be altered reproductive development. The altered development may cause altered plant phenotypes, such as altered leaf shape (particularly narrower and/or serrated and/or flat leaves); and altered phenotypes (such as altered flowering and/or changes in apical dominance and/or altered fertility). The altered development or phenotype may be caused by a change in cell proliferation.

The present invention encompasses plants or parts thereof (including seeds) obtainable by the methods according to the present invention. The plants or parts thereof comprise a nucleic acid transgene encoding a UBP15 polypeptide or a homologue thereof as defined above.

The invention also provides genetic constructs and vectors to facilitate introduction and/or expression in plants of nucleic acids encoding UBP15 polypeptides or homologues thereof. The gene constructs may be inserted into vectors, which may be commercially available, suitable for transforming into plants and suitable for expression of the gene of interest in the transformed cells. The invention also provides use of a gene construct as defined herein in the methods of the invention.

More specifically, the present invention provides a construct comprising:

-   (a) a nucleic acid encoding a polypeptide that is a member of the     UBP15 subfamily or a homologue thereof as defined above; -   (b) one or more control sequences capable of driving expression of     the nucleic acid sequence of (a); and optionally -   (c) a transcription termination sequence.

Preferably, the nucleic acid encoding the UBP15 polypeptide or a homologue thereof is as defined above. The term “control sequence” and “termination sequence” are as defined herein.

Plants are transformed with a vector comprising any of the nucleic acids described above. The skilled artisan is well aware of the genetic elements that must be present on the vector in order to successfully transform, select and propagate host cells containing the sequence of interest. The sequence of interest is operably linked to one or more control sequences (at least to a promoter).

Advantageously, any type of promoter, whether natural or synthetic, may be used to drive expression of the nucleic acid sequence. A constitutive promoter is particularly useful in the methods. Preferably the constitutive promoter is also a ubiquitous promoter. See the “Definitions” section herein for definitions of the various promoter types.

The constitutive promoter is preferably a CaMV35S promoter. Further preferably, the constitutive promoter is represented by a nucleic acid sequence substantially similar to SEQ ID NO: 52, most preferably the constitutive promoter is as represented by SEQ ID NO: 52. See Table B in the “Definitions” section herein for further examples of constitutive promoters.

Optionally, one or more terminator sequences may be used in the construct introduced into a plant. Additional regulatory elements may include transcriptional as well as translational enhancers. Those skilled in the art will be aware of terminator and enhancer sequences that may be suitable for use in performing the invention. An intron sequence may also be added to the 5′ untranslated region (UTR) or in the coding sequence to increase the amount of the mature message that accumulates in the cytosol, as described in the definitions section. Other control sequences (besides promoter, enhancer, silencer, intron sequences, 3′UTR and/or 5′UTR regions) may be protein and/or RNA stabilizing elements. Such sequences would be known or may readily be obtained by a person skilled in the art.

The genetic constructs of the invention may further include an origin of replication sequence that is required for maintenance and/or replication in a specific cell type. One example is when a genetic construct is required to be maintained in a bacterial cell as an episomal genetic element (e.g. plasmid or cosmid molecule). Preferred origins of replication include, but are not limited to, the f1-ori and colE1.

For the detection of the successful transfer of the nucleic acid sequences as used in the methods of the invention and/or selection of transgenic plants comprising these nucleic acids, it is advantageous to use marker genes (or reporter genes). Therefore, the genetic construct may optionally comprise a selectable marker gene. Selectable markers are described in more detail in the “definitions” section herein. The marker genes may be removed or excised from the transgenic cell once they are no longer needed. Techniques for marker removal are known in the art, useful techniques are described above in the definitions section.

The invention also provides a method for the production of transgenic plants having altered growth and/or development relative to control plants, comprising introduction and expression in a plant of any nucleic acid encoding a UBP15 polypeptide or a homologue thereof as defined hereinabove.

More specifically, the present invention provides a method for the production of transgenic plants having altered growth and/or development, which method comprises:

-   (i) introducing and expressing in a plant or plant cell a UBP15     polypeptide-encoding nucleic acid; and -   (ii) cultivating the plant cell under conditions promoting plant     growth and development.

The nucleic acid of (i) may be any of the nucleic acids capable of encoding a UBP15 polypeptide or a homologue thereof as defined herein.

The nucleic acid may be introduced directly into a plant cell or into the plant itself (including introduction into a tissue, organ or any other part of a plant). According to a preferred feature of the present invention, the nucleic acid is preferably introduced into a plant by transformation. The term “transformation” is described in more detail in the “definitions” section herein.

The genetically modified plant cells can be regenerated via all methods with which the skilled worker is familiar. Suitable methods can be found in the abovementioned publications by S. D. Kung and R. Wu, Potrykus or Hofgen and Willmitzer.

Generally after transformation, plant cells or cell groupings are selected for the presence of one or more markers which are encoded by plant-expressible genes co-transferred with the gene of interest, following which the transformed material is regenerated into a whole plant. To select transformed plants, the plant material obtained in the transformation is, as a rule, subjected to selective conditions so that transformed plants can be distinguished from untransformed plants. For example, the seeds obtained in the above-described manner can be planted and, after an initial growing period, subjected to a suitable selection by spraying. A further possibility consists in growing the seeds, if appropriate after sterilization, on agar plates using a suitable selection agent so that only the transformed seeds can grow into plants. Alternatively, the transformed plants are screened for the presence of a selectable marker such as the ones described above.

Following DNA transfer and regeneration, putatively transformed plants may also be evaluated, for instance using Southern analysis, for the presence of the gene of interest, copy number and/or genomic organisation. Alternatively or additionally, expression levels of the newly introduced DNA may be monitored using Northern and/or Western analysis, both techniques being well known to persons having ordinary skill in the art.

The generated transformed plants may be propagated by a variety of means, such as by clonal propagation or classical breeding techniques. For example, a first generation (or T1) transformed plant may be selfed and homozygous second-generation (or T2) transformants selected, and the T2 plants may then further be propagated through classical breeding techniques. The generated transformed organisms may take a variety of forms. For example, they may be chimeras of transformed cells and non-transformed cells; clonal transformants (e.g., all cells transformed to contain the expression cassette); grafts of transformed and untransformed tissues (e.g., in plants, a transformed rootstock grafted to an untransformed scion).

The present invention clearly extends to any plant cell or plant produced by any of the methods described herein, and to all plant parts and propagules thereof. The present invention extends further to encompass the progeny of a primary transformed or transfected cell, tissue, organ or whole plant that has been produced by any of the aforementioned methods, the only requirement being that progeny exhibit the same genotypic and/or phenotypic characteristic(s) as those produced by the parent in the methods according to the invention.

The invention also includes host cells containing an isolated nucleic acid encoding a UBP15 polypeptide or a homologue thereof as defined hereinabove. Preferred host cells according to the invention are plant cells. Host plants for the nucleic acids or the vector used in the method according to the invention, the expression cassette or construct or vector are, in principle, advantageously all plants, which are capable of synthesizing the polypeptides used in the inventive method.

The methods of the invention are advantageously applicable to any plant. Plants that are particularly useful in the methods of the invention include all plants which belong to the superfamily Viridiplantae, in particular monocotyledonous and dicotyledonous plants including fodder or forage legumes, ornamental plants, food crops, trees or shrubs. According to a preferred embodiment of the present invention, the plant is a crop plant. Examples of crop plants include soybean, sunflower, canola, alfalfa, rapeseed, cotton, tomato, potato and tobacco. Further preferably, the plant is a monocotyledonous plant. Examples of monocotyledonous plants include sugarcane. More preferably the plant is a cereal. Examples of cereals include rice, maize, wheat, barley, millet, rye, triticale, sorghum and oats.

The invention also extends to harvestable parts of a plant such as, but not limited to seeds, leaves, fruits, flowers, stems, roots, rhizomes, tubers and bulbs. The invention furthermore relates to products derived, preferably directly derived, from a harvestable part of such a plant, such as dry pellets or powders, oil, fat and fatty acids, starch or proteins.

According to a preferred feature of the invention, the modulated expression is increased expression. Methods for increasing expression of nucleic acids or genes, or gene products, are well documented in the art and examples are provided in the definitions section.

As mentioned above, a preferred method for modulating expression of a nucleic acid encoding a UBP15 polypeptide or a homologue thereof is by introducing and expressing in a plant a nucleic acid encoding a UBP15 polypeptide or a homologue thereof; however the effects of performing the method, i.e. altered plant growth and/or development may also be achieved using other well known techniques, including but not limited to T-DNA activation tagging, TILLING, homologous recombination. A description of these techniques is provided in the definitions section.

The present invention also encompasses use of nucleic acids encoding UBP15 polypeptides or homologues thereof as described herein and use of these UBP15 polypeptides in altering growth and/or development in plants.

Nucleic acids encoding UBP15 polypeptide described herein, or the UBP15 polypeptides themselves, may find use in breeding programmes in which a DNA marker is identified which may be genetically linked to a UBP15 polypeptide-encoding gene. The nucleic acids/genes, or the UBP15 polypeptides themselves may be used to define a molecular marker. This DNA or protein marker may then be used in breeding programmes to select plants having altered growth and/or development as defined hereinabove in the methods of the invention.

Allelic variants of a UBP15 polypeptide-encoding nucleic acid/gene may also find use in marker-assisted breeding programmes. Such breeding programmes sometimes require introduction of allelic variation by mutagenic treatment of the plants, using for example EMS mutagenesis; alternatively, the programme may start with a collection of allelic variants of so called “natural” origin caused unintentionally. Identification of allelic variants then takes place, for example, by PCR. This is followed by a step for selection of superior allelic variants of the sequence in question and which give altered growth and/or development. Selection is typically carried out by monitoring growth performance of plants containing different allelic variants of the sequence in question. Growth performance may be monitored in a greenhouse or in the field. Further optional steps include crossing plants in which the superior allelic variant was identified with another plant. This could be used, for example, to make a combination of interesting phenotypic features.

Nucleic acids encoding UBP15 polypeptides or homologues thereof may also be used as probes for genetically and physically mapping the genes that they are a part of, and as markers for traits linked to those genes. Such information may be useful in plant breeding in order to develop lines with desired phenotypes. Such use of UBP15 polypeptide-encoding nucleic acids requires only a nucleic acid sequence of at least 15 nucleotides in length. The UBP15 polypeptide-encoding nucleic acids may be used as restriction fragment length polymorphism (RFLP) markers. Southern blots (Sambrook J, Fritsch E F and Maniatis T (1989) Molecular Cloning, A Laboratory Manual) of restriction-digested plant genomic DNA may be probed with the UBP15-encoding nucleic acids. The resulting banding patterns may then be subjected to genetic analyses using computer programs such as MapMaker (Lander et al. (1987) Genomics 1: 174-181) in order to construct a genetic map. In addition, the nucleic acids may be used to probe Southern blots containing restriction endonuclease-treated genomic DNAs of a set of individuals representing parent and progeny of a defined genetic cross. Segregation of the DNA polymorphisms is noted and used to calculate the position of the UBP15 polypeptide-encoding nucleic acid in the genetic map previously obtained using this population (Botstein et al. (1980) Am. J. Hum. Genet. 32:314-331).

The production and use of plant gene-derived probes for use in genetic mapping is described in Bernatzky and Tanksley (1986) Plant Mol. Biol. Reporter 4: 37-41. Numerous publications describe genetic mapping of specific cDNA clones using the methodology outlined above or variations thereof. For example, F2 intercross populations, backcross populations, randomly mated populations, near isogenic lines, and other sets of individuals may be used for mapping. Such methodologies are well known to those skilled in the art.

The nucleic acid probes may also be used for physical mapping (i.e., placement of sequences on physical maps; see Hoheisel et al. In: Non-mammalian Genomic Analysis: A Practical Guide, Academic press 1996, pp. 319-346, and references cited therein).

In another embodiment, the nucleic acid probes may be used in direct fluorescence in situ hybridisation (FISH) mapping (Trask (1991) Trends Genet. 7:149-154). Although current methods of FISH mapping favour use of large clones (several kb to several hundred kb; see Laan et al. (1995) Genome Res. 5:13-20), improvements in sensitivity may allow performance of FISH mapping using shorter probes.

A variety of nucleic acid amplification-based methods for genetic and physical mapping may be carried out using the nucleic acids. Examples include allele-specific amplification (Kazazian (1989) J. Lab. Clin. Med 11:95-96), polymorphism of PCR-amplified fragments (CAPS; Sheffield et al. (1993) Genomics 16:325-332), allele-specific ligation (Landegren et al. (1988) Science 241:1077-1080), nucleotide extension reactions (Sokolov (1990) Nucleic Acid Res. 18:3671), Radiation Hybrid Mapping (Walter et al. (1997) Nat. Genet. 7:22-28) and Happy Mapping (Dear and Cook (1989) Nucleic Acid Res. 17:6795-6807). For these methods, the sequence of a nucleic acid is used to design and produce primer pairs for use in the amplification reaction or in primer extension reactions. The design of such primers is well known to those skilled in the art. In methods employing PCR-based genetic mapping, it may be necessary to identify DNA sequence differences between the parents of the mapping cross in the region corresponding to the instant nucleic acid sequence. This, however, is generally not necessary for mapping methods.

The methods according to the present invention result in plants having altered growth and/or development, as described hereinbefore. These traits may also be combined with other economically advantageous traits, such as yield-enhancing traits, tolerance to other abiotic and biotic stresses, traits modifying various architectural features and/or biochemical and/or physiological features.

EXAMPLES

The present invention will now be described with reference to the following examples, which are by way of illustration alone. The following examples are not intended to completely define or to otherwise limit the scope of the invention.

1. Plant Material and Growth Conditions

The wild-type Arabidopsis thaliana plants used in this study were of the Columbia-0 ecotype. The 38 T-DNA insertion lines (including ubp15-1, ubp15-2 and ubp19-1 those three lines with observed phenotypes) listed in Table 1 were obtained from the SALK collection. UBP15 (or UBP15C447A/S)-overexpressing transgenic plants were obtained by transforming P_(UBP15):UBP15 (or P_(UBP15):UBP15C447A/S) into wild type background. UBP15 complemented (or UBP15C447A/S) transgenic plants were obtained by transforming P_(UBP15):UBP15 (or P_(UBP15):UBP15C447A/S) into ubp15-1 background. P_(UBP19):GUS transgenic plants were obtained by transforming the P_(UBP19):GUS construct into the wild type background. ubp15 ubp16, ubp15 ubp17 and ubp16 ubp17 double mutants were obtained by crossing ubp15-1 (or ubp15-2) with ubp16-1 or ubp17-1, or by crossing ubp16-1 with ubp17-1; homozygotes of F2 generation were confirmed by PCR analysis. Triple mutants ubp15 ubp16 ubp17 were obtained by crossing ubp15 with double mutants ubp16 ubp17; homozygotes of F2 generation were confirmed by PCR analysis.

Seeds were surface sterilized with 15% (v/v) NaOCl. After 48 h at 4° C. for vernalization, seeds were placed onto 1× Murashige and Skoog (MS) plates (containing 1% sucrose, and 0.3% Phytagel) and placed in a chamber at 22° C. under continuous light for 7 days before transferring to soil. Plants were then grown in standard long day (16 h light/8 h dark) growth rooms. Seeds grown in short day (8 h light/16 h dark) conditions were sown directly onto soil and were grown in a short day condition room.

2. Sequence Alignment and Phylogenetic Analysis

The search for the common domains shared among the 27 UBP proteins was performed by TAIR and NCBI CDART. The conserved domains within each protein were joined by eliminating variant regions and by alignment of the fragments using ClustalW (Thompson et al., 1994), followed by manual alignment.

A phylogenetic tree was constructed using MAGA version 3.1 (Kumar et al., 2004) on conserved positions of the alignment, using the neighbour-joining algorithm with 1000 bootstrap replicates.

3. Measurement of the Length of Seedlings, Root, Silique and Width and Length of Rosette Leaf

To obtain the root length of seedlings, wild type, ubp15-1 and ubp15-2 were grown vertically on plates. The root length of 20 randomly selected seedlings of either wild type or mutants was determined. 20 randomly selected mature siliques (older than 8 d after pollination) of wild type or mutants were measured. Mature rosette leaves from the first true leaf to the last one was dissected from wild type or ubp15-1, and the width and length of the leaves was measured.

4. Measurement of the Flowering Time and Rosette Leaf Number

The flowering time of wild type, ubp15-1, UBP15-overexpressing line was measured as the number of days from seed germination to the opening of the first flower. Rosette leaf numbers were counted at bolting.

5. RNA Isolation and RT-PCR

RNA was isolated using Trizol (Invitrogen). Before performing RT-PCR, 4 μgs RNA was treated with RNase-Free DNase (Premega) to avoid contamination of DNA, followed by chloroform: phenol (1:1) extraction to avoid the affect of the ions. A portion of RNA was then used for PCR by At3g04120/GAPDH primers to confirm elimination of the DNA. The remaining sample was subjected to the RT reaction using a Superscript™ II RNase H⁻ Reverse Transcriptase kit (Invitrogen) and random primers. The reaction mixture was diluted 10 times and 1 μL was subjected to the PCR using rTaq DNA polymerase (TaKaRa). At3g04120/GAPDH was used as an internal control. Linearity of the PCR reaction was monitored by comparing relative amounts of PCR products after 22, 30, and 35 cycles. Forward and reverse primer sequences, used for detection of gene transcripts, were as follows At3g04120/GAPDH, 5′-CACTTGAAGGGTGGTGCCAAG-3′ and 5′-CCTGTTGTCGCCAACGAAGTC-3′; UBP15, 5′-TCGAGAGGCAACAGTTATGCTG-3′ and 5′-CTCAGGCCTCCAGTAACTGTAAGTTCTATCCTG-3′.

6. RNA Gel Blot Analysis

RNA blot was performed as previously described (Yang et al., 2005). The total RNA from different regions of leaves was extracted and 20 μgs of total RNA for each lane was separated on an agarose gel, transferred to a Hybond-N⁺ membrane (Amersham Biosciences), and hybridized with a UBP15-specific probe. 18S rRNA served as the loading control. Primers were as follows: UBP15, 5′-TCGAGAGGCAACAGTTATGCTG-3′ and 5′-CTCAGGCCTCCAGTAACTGTAAGTTCTATCCTG-3′.

7. Transient Expression in Onion Epidermal Cells

The procedure for transient expression in living onion (Allium cepa) epidermal cells using particle bombardment was performed as previously described (Ang et al., 1998). After bombardment, onion cell layers were incubated for 24 h at 22° C. in the light. The cell layers were then examined by confocal microscopy.

8. Constructs of Transgenic Lines

To obtain UBP15-overexpressing and UBP15 complemented plants, a Hindlll/Xbal-digested UBP15 promoter (1.8 kb upstream of ATG) fragment and an XbaI/StuI UBP15 CDS fragment (2.8 kb) was inserted into pCAMBIA1300 binary vector. The resulting construct was then transformed into wild type and ubp15-1 by means of Agrobacterium-mediated transformation. Constructs mutated in Cys site P_(UBP15):UBP15C447A and P_(UBP15):UBP15C447S were also made in the same way and transformed into wild type and ubp15-1. Transgenic plants were selected with hygromycin (20 μg/mL; Roche) on MS plates.

To make 35S:GFP-UBP15 (or 35S:UBP15-GFP) constructs, 35S as well as GFP-fused full-length UBP15 CDS (or full-length UBP15 CDS fused GFP) was subcloned into the XbaI/SphI site of pCAMBIA1300.

To detect tissue expression pattern of UBP19 using GUS staining, a BamHI/KpnI fragment of UBP19 promoter (1.2 kb) was inserted into pCAMBIA1381Z and transformed into a wild type background using Agrobacterium-mediated transformation. Transgenic lines were selected using hygromycin (20 μg/mL; Roche).

9. In Vitro DUB Activity Assay

The ability of UBP15 to cleave ubiquitin linked via a-amino linkages was performed in E. coli. using his-tagged substrates polyubiquitin UBQ10 and ubiquitin-extension protein UBQ1. Each of the two α-amino substrates (UBQ1 in pET28a and UBQ10 in pACYCDuet-1) were co-expressed with either GST or GST-UBP15 or GST-UBP15C447A/S in pGEX4T-3 in E. coli. strain NovaBlue (DE3) under standard conditions (22° C. induce) (Novagen). Lysates were analyzed on a Western blot with anti-ubiquitin antibody (Sigma) or anti-his antibody (Sigma). ECL chemiluminescences system (Amersham) was used for detection.

10. Tissue Fixation and Embedding for Histological Sections

To observe the transverse structure of leaves, samples were fixed for more than 24 h in FAA (50% ethanol, 5% acetic acid, and 5% formaldehyde) at room temperature, dehydrated in a graded series of mixture of H₂O: 95% alcohol: tert-butyl alcohol (4:5:1, 3:5:2, 1.5:5:3.5, 0:5:5, 0:2.5:7.5, 100% tert-butyl alcohol twice) with a 2 h incubation in each solution and then infiltrated by adding paraffin gradually (tert-butyl alcohol: paraffin as 3:1, 2:2, 1:3, 0:4, 0:4). Embedded tissues were cut into 8 μm sections with a microtome (Leica RM2255). Sections were placed onto poly-L lysine coated slides, deparaffinized and rehydrated using an ethanol series (ethanol: H₂O as 1:0, 1:0, 9.5:0.5, 9:1, 8:2, 7:3, and 1:1) with a 5 min incubation in each solution. Sections were then stained with 1% safranin O and 0.02% fast green. The cover glasses were adhibited on slides by resin. The numbers of adaxial epidermal and palisade cells were counted under a microscope.

11. Microarray Analysis and Quantitative RT-PCR

The procedures used in the microarray experiments and data analysis were described previously (Ma et al., 2002). Early emerged 9th rosette leaves of wild type and ubp15-1 were used as samples. Total RNA was isolated using RNAwiz reagent (Ambion) and purified by the RNeasy kit (Qiagen). For each sample, 50 μg of total RNA was labeled with aminoallyl-dUTP (aa-dUTP, Sigma-Aldrich) by reverse transcription. The aminoallyl-dUTP-labeled cDNAs were purified using a Microcon YM-30 filter (Millipore) and resuspended in 0.1 M NaHCO₃. The purified cDNAs were further fluorescently labeled by conjugating monofunctional Cy3 or Cy5 dye (Amersham) to the aminoallyl functional groups. Pair-wise combinations of two selected samples were used to simultaneously probe one slide, and four independent biological replicates were performed (two replicates with dyes exchange). Hybridized slides were scanned with a GenePix 4000B scanner (Axon), and independent TIFF images for Cy3 and Cy5 channels were used for subsequent analysis by GenePix Pro5.0 software package.

To confirm the microarray result, real-time PCR was performed using the ABI SYBR Green PCR master mix in a volume of 20 μL on an ABI 7900 system. The PCR mixture consisted of 0.3 μL of cDNA, 0.6 μM primers, and 1× master mix. In every real-time PCR run, At1 g42970/GAPDH was used as an internal control to normalize for variation in the amount of cDNA template. The results of a t test confirmed it to be a constitutively expressed gene. The primer sequences used were: At1 g42970/GAPDH, 5′-TCTTTCCCTGCTCAATGCTCCTC-3′ and 5′-TTTCGCCACTGTCTCTCCTCTAAC-3′. 7 genes down regulated and 2 genes up regulated were picked for quantitative RT-PCR test. Primers used to quantify those genes were At1g71030/MYB, 5′-CATTTGCCTGACCTAAACATTG-3′ and 5′-AAGCGTTTCTTGACCTGTTGA-3′; At5g57660/TRANSCR/PT FACTOR, 5′-GGCTCATCCACCACCGTT-3′ and 5′-GGGAGAGGCTCTGTTTTCGTC-3′; At5g67030/ABA 1, 5′-GGGCTTGGTCCTCTGTCTT-3′ and 5′-GTGAGTCTGCAACTAGGTGGC3′; At5g35970/HELICASE-LIKE, 5′-CCACAGGGCTCGGAGGTAT-3′ and 5′-TCGTAAGTAAGGGCATCGGC-3′; At3g49160/PYRUVATE KINASE FAMILY PROTEIN, 5′-TCCAGCAGGTCTCACATAAACAA-3′ and 5′-CTGCTGCTAAGAGATGTGACCG-3′; At1g73480/HYDROLASE, 5′-AATGGCGGTGGAAACAATG-3′ and 5′-ACGACGCGAAACGGAAGGAG-3′; At5g24470/APRR5, 5-TACCCTACGCCAACCCCTAT-3′ and 5′-ATGTGATTGCCTATTGCACTATGT-3′; At3g20810/TRANSCRIPTION FACTOR, 5′-CCTCAATGCTGTTGCTGGTAA-3′ and 5′-TGGGCAAGATAAGTAGGCTCC-3′; At4g21990/APR3, 5′-CTGTCAACACGCTTCACGC-3′ and 5′-TCTTTCCGGTTCTCTAACTTCATC-3′. To determine the specificity of those primers, the amplified products were subjected to melt curve analysis using the machine's standard method. Cycling conditions were as follows: 50° C. for 2 min, 95° C. for 10 min, 40 cycles of 95° C. for 15 s, 60° C. for 30 s, and 72° C. for 1 min. The reported values were averages of six independent trials (two biological replicates and three technical replicates). Relative expression levels were calculated as follows. Transcript levels of those genes were normalized relative to a standard (GAPDH) using the formula ΔC_(T)=C_(T (gene X) mean of technical repeat)−C_(T (GAPDH) mean of technical repeat) either in wild type or ubp15-1. Then, the ΔCt_((wild type)) and ΔCt_((ubp15-1)) of each gene was obtained. Wild type was used as the standard for the comparison of expression levels. Relative expression levels were then calculated using the equation 2^(−[ΔCT (ubp15-1)−ΔACT (wild type)]). Next, the C_(T) average of 2 biological repeats was calculated.

12. Detection of GUS Activity

P_(UBP19):GUS transgenic lines were grown on MS plates. Seedlings were washed gently with 100 mM sodium phosphate buffer, pH 7.0, and then stained for 4 h at 37° C. in 2 mM X-glucuronide dissolved in 0.1 mM potassium ferricyanide, 0.1 mM potassium ferrocyanide, 10% Triton X-100, 100 μg/ml chloramphenicol, and 500 mM sodium phosphate buffer, pH 7.0 (Weigel and Glazebrook, 2002; Byrne et al., 2003). The tissue was then washed in 100 mM sodium phosphate buffer followed by 95% and 70% ethanol at room temperature. Microscopy was performed by a dissection microscope (Leica MZFLIII) with a 10× objective, and images were captured by Canon digital camera (Power Shot S70).

13. Accession Numbers

Arabidopsis Genome Initiative locus identifiers for the genes mentioned in this article are listed in Table 1.

14. The UBP Genes Exhibited Non-Identical Expression Profiles

To obtain expression patterns of the UBP genes, a previously described microarray data set was examined covering 18 different Arabidopsis organs, including cauline leaves, rosette leaves, pistil one day before pollination, pistil one day after pollination, silique 3 day after pollination, silique 8 day after pollination, stem, sepal, stamen, petal, seed, cultured cell, root dark, root white light, hypocotyl dark, hypocotyl white light, cotyledon dark and cotyledon white light (Ma et al., 2005; Supplemental Table 1). In that described study, 24 of 27 UBP genes were covered by the microarray used and expression for all 24 genes was detected in one or more tissues. Among those 24 genes, UBP9 and UBP10 were found to be essentially identical and their oligo probes were cross-hybridized to each other, thus not enabling definitive definition of the expression of both genes. The expression of the three genes not covered by this microarray, UBP13, UBP14 and UBP20, were reported in a prior study (Yan et al., 2000). As a sample case, the tissue-specific expression profiles for the 5 genes in UBP15 subfamily were present in FIG. 13. The 5 genes appear to have distinct expression profiles.

15. Genome Wide Isolation and Analysis of T-DNA Insertional Mutants of the UBP Genes

As a first step in the functional analysis of the UBP gene family, the North America Arabidopsis Resource Center database was searched for all available T-DNA insertion lines for the UBP gene family members. A total of 38 T-DNA insertion lines corresponding to 25 UBP genes were obtained and verified, as summarized in Table 1 with the locations of the T-DNA insertion sites for each line. Following PCR-based genotyping, forward and reverse primers (Supplemental Table 2) were designed. Examination of possible phenotypes of those individual mutant homozygous lines revealed that only 5 loss-of-function mutant lines in 3 genes of 2 subfamilies exhibited visible phenotypes (Table 1). Two independent T-DNA alleles for UBP14 exhibited recessive embryo lethality, similar to a previous report (Doelling et al., 2001). Another three mutant lines belonging to the UBP15 subfamily, with two alleles for UBP15, exhibited a leaf morphology phenotype, and one allele for UBP19 exhibited embryo lethality. The 5 genes in this subfamily had not previously been characterised and so were selected for in-depth analysis.

A search for homologous genes of AtUBP15 subfamily in Rice (Oriza Sativa) to find out whether they have similar functions was carried out. Four genes were found with high similarity, and were aligned with the 5 AtUBP15 subfamily genes. The resultant phylogenetic tree is shown in FIG. 14. One of the rice genes was even more similar to AtUBP15 than other Arabidopsis genes.

16. The Two ubp15 Mutant Alleles Exhibited Similar Leaf Development Defects

The two T-DNA insertion lines for UBP15, Salk_(—)018601 and Salk_(—)015611, designated ubp15-1 and ubp15-2, were identified from the Salk collection and have T-DNA insertions in the 12th and 8th exon of the UBP15 gene respectively (FIG. 2A). Semi-quantitative RP-PCR showed the mRNA expression level could not be detected in either of the two mutants (FIG. 2B), suggesting both are null alleles. Both lines segregated a single, recessive Mendelian trait (described below) similar to each other co-segregating with the T-DNA, indicating the trait was caused by a single insertion in UBP15. Compared to wild type adult plants, both mutants give smaller plants and narrow, serrated leaves, with the leaf phenotype becoming more severe in the later rosette leaves (FIG. 2C). The mutants also exhibited shorter roots in seedling stage (FIG. 2D), smaller flowers (FIG. 2E), shorter siliques (FIG. 2F) as well as short and slim stems. Those morphopmetric changes (silique length, root length, primary stem length and primary stem diameter) are summarized in Table 2.

The morphology of rosette leaves using ubp15-1 were further analysed. The rosette leaves of wild type Arabidopsis grown in long day condition (16 h light/8 h dark) gradually change their overall patterns, starting with true leaves round and flat, slowing become more ovule shaped and a little downward-curled, eventually become long and narrow shape, with severe downward-curled margin. While the rosette leaves of ubp15-1 mutants are more flat even at a later stage and consistently produce fewer rosette leaves (10.8 versus 12.6 of wild type) before bolting (FIG. 2C). The ratio of length and width of ubp15-1 and wild type was plotted and defined as a leaf index value (Tsukaya, 2006), and revealed a much stronger reduction in width than in length of the rosette leaf blade in the mutant (FIG. 2G). On the contrary, cauline leaves of ubp15-1 did not show any obvious difference compared to the wild type.

Consistent with the reduced number of vegetative leaves, ubp15-1 also exhibited an early flowering phenotype, with average flowering time of 39.1 (±2.02) days versus the 41.5 (±3.79) days for wild type (Table 2). Even in short day condition (8 h light/16 h dark), ubp15-1 was also slight early flowering (Table 2). Also noted was that ubp15-1 rosette leaves had less weight (Table 2) and were thinner, implying alteration of the cell structure.

17. UBP15 Expressed Highly in Rosette Leaves and Reproductive Tissues, and Localized to Both Cytosol and Nucleus

The presence of defects in ubp15-1 rosette leaves and flowers suggested involvement of UBP15 in regulation of vegetative and reproductive development. To support this, and to verify the prior microarray analysis, a semi quantitative RT-PCR was employed to examine tissue specific expression of UBP15. As shown in FIG. 3A, the mRNA level of UBP15 was highly accumulated in the rosette leaves and inflorescences, while low in roots, siliques and cotyledons, intermediate level in stems and cauline leaves. This expression pattern is largely consistent with microarray data (Supplemental Table 1 and FIG. 13).

The spatial expression pattern of UBP15 within a rosette leaf was further examined. As in FIG. 3B, rosette leaves at early, middle, and late stages were selected and dissected into center and margin regions for separate RNA preparations (FIG. 3B upper part, shown by the black lines) and RNA blot analysis (FIG. 3B, bottom). UBP15 mRNA level increased from early leaf to late leaf, together with a more evident higher expression in margin of leaf in late stage. These leaf expression patterns during development were consistent with a role of UBP15 in defining the leaf pattern and shapes of leaves margin, such as serrating and curling.

To assess the subcellular distribution of UBP15, constructs containing either 35S:GFP-UBP15 or 35S:UBP15-GFP were transformed into onion epidermal cell. Transient expression showed the fusion proteins ubiquitously present in both cytosol and nucleus, and the result for 35S:GFP-UBP15 is shown in FIG. 3C.

18. UBP15 Possess De-Ubiquitinatination Activity in Vitro and this Biochemical Activity is Essential for Function in Vivo

To verify UBP15 is a bona fide de-ubiquitinating enzyme, UBP15 as well as two mutated forms (changed the conserved catalytic center Cysteine⁴⁴⁷ residue to Alanine or Serine) were co-expressed as GST fusion proteins in E. coli. The his tagged UBQ1 or UBQ10 poly-ubiquitin proteins were used as substrates for in vitro DUB activity assay with recombinant GST-UBP15 wild type or mutant form proteins. Immunoblot analysis with anti-ubiquitin antibody showed UBP15 was capable of cleaving the two substrates and that Cysteine⁴⁴⁷ is essential for this DUB activity (FIGS. 4A and 4B respectively).

To test the essential role of DUB activity of UBP15 in plant development, we introduced wild type UBP15 and its two Cysteine⁴⁴⁷ mutant forms under the control of the UBP15 native promoter into wild type Arabidopsis and ubp15-1 background by means of Agrobacterium-mediated transformation. For the transgenic lines with wild type background, we obtained in total 36 independent T₀ generation plants for the wild type UBP15 transgene. Half of the lines (18 out of 36) exhibited no phenotypic changes, whereas the other half displayed interesting differences from wild type, opposite to the ubp15 mutant phenotypes (FIG. 4C, middle left). For those lines with wild type transgenes in ubp15-1 background, 5 independent lines showed wild type phenotype (FIG. 4C, middle right), thus functionally rescued the mutant defect. RNA gel blot analysis with two representative lines from each groups (FIG. 4D) revealed that high level expression of the transgene in wild type background was responsible for the abnormal phenotype opposite to ubp15-1 mutant, while expression level similar to endogenous gene confer phenotype rescue in ubp15-1 mutant and no phenotype effect in wild type background. Where the wild type transgene failed to rescue the ubp15-1 phenotype, those transgenic lines only expressed truncated ubp15 mRNA and failed to express wild type mRNA.

Introduction of UBP15C447A or UBP15C447S mutant transgenes under the control of the UBP15 native promoter into wild type, and ubp15-1, failed to cause overexpression phenotype in wild type background and complementation of mutant phenotype in ubp15-1 background, as the RNA gel blot analysis showed normal or even higher level expression of mutant genes (FIGS. 4C and 4E). In contrast, some lines with UBP15C447A in wild type exhibited phenotype similar to ubp15-1 mutant (FIG. 4C, bottom left, and 4E), which was opposite to the UBP15-overexpression in wild type background, as did transgenic lines of wild type overexpressing UBP15C447S (data not shown). Those lines tended to express the mutant transgene at higher levels, likely caused a dominant negative interference with endogenous protein function. These results imply that DUB activity is essential for UBP15 function in vivo.

19. Over-Expression of UBP15 Displaying Phenotypes Opposite to ubp15-1 Mutants

We further examined the phenotypes of UBP15-overexpressing lines (wild type transgenes in wild type background) above. One obvious phenotype was the larger overall status of the plants as well as each rosette leaf. The rosette leaves of those over-expressing lines were rounder than of wild types starting at very early stage and were severely downwardly-curled in the middle to later stages (FIG. 4C, middle left). Later developed rosette leaves, such as the ninth rosette leaf, were not only downwardly-curled, but also sometimes displayed a knot in the leaf tip region (arrow in FIG. 5B, compare 5A and 5B), possibly caused by the uneven proliferation of the cells in different positions within a leaf. In addition, the UBP15-overexpressing line was also late flowering, with the greater number of rosette leaves (16.2) before bolting than that of wild type, and the delay in flowering time under long day conditions (Table 2). The fresh weight of the rosette leaves of UBP15-overexpressing lines per area was also increased compared to wild type (Table 2).

There was also an evident flower phenotype in UBP15-overexpressing lines. Compared to the wild type, UBP15-overexpressing lines exhibited larger flowers (compare FIGS. 5I and 5J) with a high rate of abnormality in petal or stamen number (by 91.3%, 40 out of 46 in one plant) in the early flowers (FIGS. 5C and 5D, 5E, 5K). However this flower pattern abnormality was less frequent in late flowers. The overexpression lines also has siliques larger than wild type (FIG. 5L), opposite to the ubp15-1 mutants. Flower and silique abnormalities do not affect fertility, unless in extreme cases where damaged sexual organs prevented fertilization (FIG. 5H and 5M). An increased apical dominance in over-expressing lines was seen compared to the reduce apical dominance in ubp15 mutants (Table 2 and FIG. 15). In some extreme cases of UBP15 over-expression plants, positions for expected secondary bolts in the only main bolt degenerated into a flower then silique (FIG. 5G) contrasting to wild type (FIG. 5F).

20. The Ubp15 Loss-of-Function Mutants and UBP15-Overexpressing Plants Display Opposite Abnormality in Leaf Cell Proliferation

To further characterize the role of UBP15 in Arabidopsis leaf development, the morphogenetic patterns of all leaves, from cotyledons, true leaves, to cauline leaves from loss-of-function mutants, over-expressing plants, and wild type were compared. As shown in FIG. 6A, wild type plants had about 11 rosette leaves, while both two ubp15 mutants had about 9 rosette leaves. In contrast, UBP15-overexpressing line produced about 14 rosette leaves. Rosette leaves in the two mutants were narrow, serrated and flat, but were more round in early leaves and downwardly-curled in later leaves in UBP15-overexpressing plants. The cauline leaves did not exhibit obvious differences amongst those lines examined, except two mutants had slightly narrower leaves.

To examine the cellular basis for their small plant size and narrow leaf lamina of the ubp15 mutants, transverse sections of leaves from mutants as well as UBP15-overexpressing line were compared with wild type leaves. The cartoon in the right of FIG. 6B illustrates the positions of representative sections routinely obtained and analyzed, which was in the middle region of the leaf. The left cartoon in FIG. 5B was the section model of the middle region of wild type. Six leaves (leaves with odd numbers in FIG. 6A) were selected for measurement, from the first cotyledon to the first, the third, the fifth, the ninth true leaf and the first grown cauline leaf. Those true leaves later than the ninth were not included for uniformity, because two mutants produced only 9˜10 true leaves. Adaxial epidermal cell number and palisade cell numbers in each line were counted in serial sections (3˜4) under microscope.

For adaxial epidermal cells, the cell number of each position in each line is shown in FIG. 6C. At the beginning of leaf development, the adaxial epidermal cell numbers across the lamina among those lines was similar, which was ˜30 cells in the cotyledon of each line, but the difference increased with the development of the leaves, and severely differed in the ninth rosette leaf, cell numbers across the lamina of which were ˜290 in wild type, ˜180 in two mutants (decreased by ˜40%) and ˜400 in UBP15-overexpressing line (increased by ˜40%). It was consistent with the phenotype observed, for distinction became noticeable in late development phases. Adaxial epidermal cell number of cauline leaf was higher than that of any rosette leaves. This may possibly be caused by more density in the adaxial epidermal cell number across the cauline leaf. Similar results were observed in the measuring of palisade cell number (FIG. 16). Mutation of UBP15 gave a decrease in adaxial epidermal and palisade cell number in a lateral direction, while overexpression of UBP15 led to the opposite.

21. Arabidopsis UBP15 is Involved in Leaf Cell Layer Organization

To extend the findings of cell number alteration, the cellular structure of the leaves of those lines was examined. Based on the result that late developed rosette leaves exhibited severe phenotype, the fully expanded ninth rosette leaf was chosen for comparison of the transverse sections of cellular structure in the middle region of the lines (FIG. 6B). As FIG. 7A left first wild type shown, leaf had an organized internal anatomy containing a layer of vertically packed palisade cells beneath the adaxial surface, and ˜4 layers spongy parenchyma cells, interspersed with air spaces, were loosely arranged below the palisade layer. ubp15-1 and ubp15-2 also exhibited similar structure but the number of spongy cell layers in mutants was less than that of wild type, whereas that of UBP15-overexpressing line was more (FIG. 7A, from left, the second to the fourth). The spongy cell layers in wild type was generally ˜4, but in two mutants the spongy cell layers were ˜3, while in UBP15-overexpressing line the spongy cell layers reached ˜5. The defects in cell layer structure in ubp15-1 was rescued by expression of its corresponding wild-type UBP15, confirming that these ubp15-1 phenotype was caused directly by disruption of the UBP15 gene (data not shown). These results were consistent with the fresh weight results for less weight corresponding to the less cell layers (Table 2), greater weight resulting from more cell layers (see above). A slight increase in the cell size of mutants was detected, implying partial compensation of the loss of cell number.

The mid-vein and peripheral structure of those lines was also compared. The vascular bundle of wild type was composed of several layers of xylem and phloem surrounded by layers of parenchyma cell (FIG. 7B, left first). In contrast, two mutants showed decreased thickness. The vascular bundles of the two mutants were slimmer than of the wild type due to decreased cell number in xylem and phloem. In addition, the numbers of parenchyma cells surrounding the vascular bundles of two mutants was also reduced. In UBP15-overexpressing line, opposite results were obtained, showing advanced vascular bundle, strong both in xylem and phloem (FIG. 7B, from left, the second to the fourth).

22. Transcriptome Analysis Shows UBP15 Influences Expression Level of 804 Genes (Adjusted P<0.15)

To examine the cell cycle effects in ubp15-1 and to explore the possible role of UBP15 in regulating the transcription of other genes, we performed microarray assay to conduct a genome wide expression analysis on the ninth rosette leaf immediately emerged. Microarray analysis also confirmed no expression of UBP15 mRNA in ubp15-1 (Supplemental Table 3). Statistical analysis showed a total of 804 out of 20,000 genes were differentially expressed in ubp15-1 compared with wild type at adjusted P<0.15 (4% of the expressed genes), among which 406 (50.5%) were up regulated and 398 (49.5%) were down regulated with fold change expression ranging from 1.72 to 8.35 and 0.09 to 0.56, respectively (Supplemental Table 3). To confirm the trends observed in the transcriptome analysis, we randomly picked 9 genes with 7 down regulated and 2 up regulated and performed real-time PCR. Expression levels of those genes was consistent with that of microarray result at 100% (FIG. 8), suggesting microarray assay was reliable. At1g42970/GAPDH served as an internal control.

To characterize the biological processes involved, representatives of those genes influenced by the ubp15-1 mutant were analyzed for gene ontology (GO) (Maere et al., 2005) (Table 3). Two genes related to cell cycle were differentially expressed in ubp15-1 (Table 3). Because the flowering time was also influenced in ubp15-1, genes controlling flowering were the focus. Floral homeotic gene CAL, positively regulating flower development, was up regulated 1.98 fold in ubp15-1 background, while another one, MAF5, negatively regulated flower development was down regulated 0.31 fold (Table 3).

Other categories influenced by ubp15-1 comprised genes involved in biosynthetic metabolism, chlorophyll biosynthesis, photosynthesis, signal transduction and also included a large number of transcription factors (Table 3). Thus, besides effects on some phenotype-related genes such as cell cycle and flowering control, the ubp15-1 mutant was in general defective in numerous plant metabolism pathways at the transcriptional level, suggesting secondary and not only primary effects on the observed growth defects.

23. UBP15 and UBP16 are Partially Redundant but not with UBP17

UBP16 and UBP17 are two closely related proteins (FIG. 1), suggesting they may have functional redundancy. Knockout lines of the two genes (ubp16-1, ubp17-1 and ubp17-2) (FIG. 9A) did not show any observable phenotype. ubp16-1 was crossed with ubp17-1 or ubp17-2 to examine whether there was any defect in double mutants. Homozygote F2 generation of crossed lines did not show noticeable phenotype, indicating there may be other proteins for redundancy. Subsequently crossed were ubp15 mutants with the double mutant ubp16 ubp17. In the F2 generation, three gene types of double mutants ubp15 ubp16, ubp15 ubp17 and ubp16 ubp17 were obtained, as well as a triple mutant ubp15 ubp16 ubp17 (FIGS. 9B and 9C, ubp16 ubp17 not shown). Double mutant ubp15 ubp16 showed a similar but more severe phenotype to the ubp15 mutant, indicating there may be functional redundancy of the two genes. ubp15 ubp16 exhibited dwarf plants and aborted siliques, rosette leaves, which were narrower than that of ubp15 mutants (FIG. 9C). The alteration in cellular level was also conspicuous, only 2 spongy cell layers (FIG. 7A, right first) and strikingly degenerated vascular bundle (FIG. 7B, right first). In the case of the ninth leaf, the adaxial epidermal cell number cross the leaf lamina decreased by 60% over that of wild type (FIG. 17), as did the palisade cell number (data not shown). In contrast, ubp15 ubp17 did not further the defect of ubp15 mutants, implying those two gene may work in two different pathways to regulate cellular function. The triple mutant ubp15 ubp16 ubp17 was similar to the double mutant ubp15 ubp16, further confirming UBP17 involves in another regulating pathway from UBP15 and UBP16, although it had higher sequence homology to UBP16.

The data suggest that the UBP15 mutation disrupted rosette leaf development, and its effect was more prominent when combined with UBP16. The effect of UBP16 was only detectable in the presence of UBP15. There was no detectable effect of the UBP17 mutation on this process. These results indicate that UBP15 is a major regulator of the shape of rosette leaves and development of the whole plants. UBP16 is also involved in these processes, although its contribution was less prominent than that of UBP15.

24. UBP19 May be Involved in Embryo Development While the Function of UBP18 is Unknown

FIG. 9A shows UBP18 and UBP19 gene structure with two T-DNA mutants each. ubp19-1, with T-DNA inserted in the 5′UTR region 195 bp upstream of ATG, exhibited recessive embryo lethality, with ˜1/4 (13/47) aborted embryos in one heterozygote silique (FIG. 9B, arrow indicated yellow embryos). Further statistical analysis of an average of 10 siliques in each heterozygote line showed the ratio of the normal:abnormal was ˜3:1 (372/136), confirming it was a recessive embryo lethal line. The embryo development in a specific heterozygote silique, from mature stage tracing back to globular stage was examined. It was found that ubp19-1 stopped developing at globular stage (FIG. 10C).

It is therefore proposed that UBP19 is involved in early stage embryo development. A GUS construct driven by a 1.2 kb UBP19 promoter was made to transform wild types and to examine tissue expression pattern. It was found that UBP19 was ubiquitously expressed, including in the whole young seedling, except the root meristemetic region (FIG. 11A) (Enlarged in FIG. 11A was the detailed demonstration of root tip region), in the vascular tissues and stomas of mature rosette leaves (FIG. 11B) as well as in inflorescence. Detailed examination found GUS expressed in the sepal and petal vascular tissues, also in anthers and styles (FIG. 11C). GUS was detected in the tip and basal regions of siliques but hardly within the embryos (FIG. 11D).

Another ubp19 mutant, 205 bp upstream of ATG, did not show any obvious phenotype, indicating the region between 195 bp to 205 bp upstream of ATG was essential for the function of UBP19.

Neither of the two mutants inserted in UBP18 exon and intron exhibited any observable phenotype, implying potential functional redundancy between UBP18 and other proteins in this family.

25. UBP15 is Involved in Rosette Leaf Development

Phenotype of ubp15 mutants and UBP15-overexpressing lines provided a basis for further analysis of this gene in plant leaf development. Both ubp15 mutants showed rosette leaves that were narrow, serrated and flat, whereas UBP15-overexpressing lines produced an opposite phenotype with rosette leaves that were round (early developed) and downwardly-curled (late developed) (FIG. 2A and FIG. 5B). The cell number of transverse sections (both palisade and adaxial epidermal cells across the leaf lamina) of ubp15 mutants decreased whereas that of UBP15-overexpressing line dramatically increased compared to wild types. This indicates that UBP15 alters leaves shape by cell proliferation, possibly by regulating cell cycle proteins. Recently, hub1 was found to exhibit narrower rosette leaves, caused by cell number decrease and a microarray assay discovered that the amount of genes related to cell cycle and cytokinesis were changed (Fleury et al., 2007). In this study, although microarray data showed there were only two genes related to cell cycle altered (ICK1 and Cycle-like F box domain containing protein), their expression level was consistent with the cell number decrease. The rosette leaves in mutants became flat while they were downwardly-curled in UBP15-overexpressing lines. The expression level of UBP15 in rosette leaves increased in the leaf margin with the development of plants (FIG. 3B), suggesting that UBP15 specifically (at least partly) determines the margin of rosette leaves. This was similar to iamt1-D, which displayed dramatic hyponastic leaf phenotypes caused by increased expression levels of the IAMT1 gene, and which was found to be specifically expressed in the margin of rosette leaves by GUS expression assay (Qin et al., 2005).

The leaf index increased in ubp15-1 mutants because of narrower rosette leaves (although leaf length was shorter but less altered and lead to a large leaf index value). Polarized growth of leaf blades in the leaf-width direction is governed by polar elongation of leaf cells or polar cell proliferation (Tsukaya, 2006). Genes altered cell proliferation in leaf-width direction reported until now are GIF1 (also named AN3) (Kim and Kende, 2004), GRF5 (Horiguchi et al., 2005), and HUB1 (Kim and Kende, 2004; Horiguchi et al., 2005; Fleury et al., 2007). They all are important in positive control of cell number in leaf width direction. ubp15 mutants altered adaxial epidermal and palisade cell numbers in leaf width direction, but microarray data did not show there was any change of the expression level of GIF1 (AN3), GRF5 or HUB1 in ubp15-1 background. This may because of distinct pathways involved by UBP15 and those genes.

26. The Cysteine Amino Acid of UBP15 is Critical for its Function in Vitro and in Vivo

In vitro co-expression assay showed UBP15 is a bona fide ubiquitin specific protease and Cys⁴⁴⁷ is critical for this activity. It was found that UBP15 can only cleave a-linked peptide (polyubiquitin and ubiquitin-extension gene) (FIG. 5A), not c-linked isopeptide (multiubiquitin chain linked by iso-peptide) (data not shown), suggesting it may only function on a-linked peptide or can only recognize the site of substrate-proximal end of the chain. UBP3, 4 and 5 proteins were reported to contain nuclear localization signal and were deduced to only function on isopeptide-linked substrates (Chandler et al., 1997; Rao-Naik et al., 2000). The subcellular localization of UBP15, ubiquitous expression throughout the cell, suggests that this enzyme may recognize more than one substrate to execute its diverse functions; or it has other function addition of de-ubiquitination.

In this study, we first proved in vivo function of Cys⁴⁴⁷ of UBP15 in leaf development. While expressing UBP15 wild type construct in ubp15-1 can rescue the mutant phenotype, neither overexpressing UBP15C447A or UBP15C447S showed complementation of mutant deficiency. This implied Cysteine⁴⁴⁷ was the functional residue of UBP15. On the other hand, transgenic lines of wild type with constructs containing wild type UBP15 exhibited downwardly-curled mature rosette leaves while those with constructs containing mutation in Cys447Ala or Cys447Ser showed ubp15-1 mutant phenotype. This result confirmed the phenotype of rosette leaves was caused by overexpression of UBP15 and that the Cys⁴⁴⁷ is critical for this function. It also implies that it is the de-ubiquitination activity but not other domains (such as Zinc finger MYND) that cause the abnormality. Recently found gene HUB1 (Fleury et al., 2007), an E3 ligase mono-ubiquitinating H2B, with similar phenotype as ubp15 mutants, possibly shares the same pathway as UBP15.

There is also another result that transgenic lines with construct containing UBP15 driven by 35S promoter in wild type background did not show any phenotype, nor did the mutant can be rescued (data not shown). This suggested the native promoter may provide a favorable spatial structure for better executing the function of exogenous proteins.

27. UBP15 Regulates Transcription of Many Genes

A microarray assay was performed to analyze the possible role of UBP15 in regulating other genes at a transcriptional level. Two genes related to cell cycle were found to be altered and may directly cause the cell number changes in ubp15-1, although not like HUB1, which altered cell cycle proteins across the genome (24 genes).

We also found two genes controlling flowering were altered and this alteration caused the phenotype we observed. MAF5 and Floral homeotic gene CAL, regulate flowering in opposition, both showed altered ubp15-1 and caused the early flower phenotype.

Although numerous other genes were up- or down-regulated in ubp15-1, they seem to be the secondary effectors instead of proximal downstream targets.

28. Functional Redundancy Among the UBP15 Subfamily Members

UBP15 subfamily members encode proteins containing zinc finger MYND domains. They can be further divided into 3 groups based on the sequence similarity. UBP16 and UBP17 have 50% amino acid identity in their two conserved domains, while UBP18 and UBP19 have 68% identity in the full length. But UBP15 is less similar to other four (UBP15 to UBP16 is 37% identity in the UBP domain and to UBP18 is 45% identity in the full length), and this explains the ubp15 mutant phenotype. To see if UBP16 and UBP17 have functional redundancy, the two mutants of the two genes were crossed to give double mutants. Homozygotes of double mutants did not show any phenotype suggesting they may work in different pathways. Subsequently, the double mutant was crossed with ubp15 mutants to examine whether there is any alteration. In the F2 generation, only ubp15 ubp16 but no others intensified the phenotype of ubp15 mutants. This indicated that UBP15 and UBP16 may have functional redundancy. Triple mutant ubp15 ubp16 ubp17 exhibited similar phenotypes as ubp15 ubp16 further suggesting UBP17 did not involve in the function shared by the other two. On the other hand, ubp16 mutant did not display any visible phenotype, but it intensified the phenotype of ubp15 mutants, suggesting that in Arabidopsis, UBP15 is a master regulator in this pathway. Functional redundancy was also observed in another subfamily UBP1 and UBP2, whose double mutants but not each mutant were sensitive to Canavanine (Yan et al., 2000).

The sequence homology of UBP18 and UBP19 also imply functional redundancy. However, only one mutant (ubp19-1) out of four showed recessive embryo lethality. Furthermore, insertion in the 195 bp upstream of UBP19 5′UTR caused a phenotype, whereas inserting 205 bp upstream of UBP19 5′UTR did not show any phenotype. This implies the region from 195 bp tracing to 205 bp upstream of UBP19 5′UTR is critical for the function of UBP19.

On the other hand, although UBP16 and UBP17 are more related to each other than to UBP15 in protein sequences, the exhibited phenotype of ubp15 ubp16 similar to ubp15 mutant suggested UBP16 was more related to UBP15 instead of UBP17 in function. This also applies to the group of UBP18 and UBP19, since the phenotype can only be detected in the ubp19 mutant but not in ubp18 mutants. This shows that proteins closely related at a sequence level are not always functionally redundant.

DESCRIPTION OF FIGURES

The present invention will now be described with reference to the following figures in which:

FIG. 1. Phylogenetic Analysis of 27 UBPs family of Arabidopsis.

The Phylogenetic tree of 27 UBPs. The branch lengths of the tree are proportional to divergence. The 0.1 scale represents 10% change. Bootstrap values are shown in percentages at nodes. 27 proteins can be subdivided into 14 subfamilies differing in distinct colors based on the domain similarity. Multiple alignments used for this analysis are shown in FIG. 12.

Proteins with conserved domains are plotted on a schematically scale. Each colored box represents a domain. Black lines represent the length of UBP proteins, while the length of the domains can be estimated by the binding black lines. aa, amino acids; UBP, ubiquitin specific protease; ZnF, zinc finger; MYND, myeloid, Nervy, and DEAF-1; DUSP, domain in ubiquitin-specific proteases; UBQ, ubiquitin homologues; MATH, meprin and TRAF homology; UBA, ubiquitin-associated.

FIG. 2. Characterization of the Ubiquitin-Specific Protease gene UBP15.

-   (A) Gene structure of UBP15. There are 14 exons dispersed within the     4.37 kb genomic region. Black boxes represent the exons while lines     between those exons are introns. White boxes in the two ends stand     for 5′ and 3′ UTRs. Two T-DNA knockout lines inserted in the 8th and     12th exon respectively, each resulting in destroyed UBP domain. -   (B) Expression of UBP15 in the wild type and the homozygous ubp15-1     and ubp15-2 by RT-PCR with the primer of UBP15FP and UBP15RP.     At3g04120/GAPDH served as an internal control. -   (C) One-month-old plants of wild type, homozygous ubp15-1 and     homozygous ubp15-2. Bar=1 cm. -   (D) 12-d-old seedlings of wild type, homozygous ubp15-1 and     homozygous ubp15-2. Bar=1 cm. -   (E) Flowers of wild type, homozygous ubp15-1 and homozygous ubp15-2.     Bar=1 mm. -   (F) Siliques of wild type, homozygous ubp15-1 and homozygous     ubp15-2. Bar=1 cm. Plants above all grow in 16 light/8 dark     condition. -   (G) Length and width ratio of the rosette leaves of wild type and     ubp15-1 in short day condition (8 h light/16 h dark). Error bars     represent the standard deviation of the 7 repeats.

FIG. 3. Tissue and developmental expression patterns of UBP15, and subcellular localization of UBP15 in onion epidermal cells.

-   (A) RT-PCR analysis of tissue expression pattern of UBP15.     At3g04120/GAPDH as an internal control. -   (B) Northern blot analysis of UBP15 expression pattern in leaf     center and margin regions in three developmental stages, P1, P2 and     P3. Leaves were dissected in two parts: center and margin as the     lines shown in the figure. Equal amounts of total RNA from the     different samples were used, and gel blot was hybridized and labeled     with UBP15 gene-specific probes. The rRNA band pattern was used to     show equal loading. C, center region; M, margin region. Bar=1 cm. -   (C) Subcellular localization of UBP15 in onion epidermal cells.     Bar=100 μm.

FIG. 4. UBP15 encodes a functional deubiquitinating enzyme capable of cleaving the polypeptides, and its Cys⁴⁴⁷ is essential for the function in vitro and in vivo.

-   (A) UBP15 can cleave substrate UBQ1 (ubiquitin-extension protein).     Co-expressed plasmids in E. coli. Novablue (DE3) strain (Novagen)     was UBQ1 with GST vector (lane 1), GST-UBP15 (lane 2),     GST-UBP15C447A (lane 3) and GST-UBP15C447S (lane 4). The cleaved     products were detected by immunoblot analysis with anti-ubiquitin     antibody. -   (B) UBP15 can cleave substrate UBQ10 (hexameric polyubiquitin).     Co-expressed plasmids in E. coli. Novablue (DE3) strain (Novagen)     was UBQ10 with GST vector (lane 1), GST-UBP15 (lane 2),     GST-UBP15C447A (lane 3) and GST-UBP15C447S (lane 4). The cleaved     products were detected by immunoblot analysis with anti-ubiquitin     antibody. Cleaved products are shown as white arrows. -   (C) Expression of UBP15 in ubp15-1 recapitulates its wild type     function, while overexpression of UBP15, but not UBP15C447A or     UBP15C447S, causes phenotype with round (early developed) and curled     down (mature) rosette leaves opposite to the ubp15-1 mutants.     Samples one-month-old from left to right and up to bottom are: wild     type, ubp15-1, UBP15-overexpressing line, UBP15-complemented line,     UBP15C447A-overexpressing line and UBP15C447A-overexpressing in     ubp15-1 line. Bar=1 cm. -   (D) RNA gel blot analysis of the UBP15 gene expression in transgenic     lines. RNA levels from wild type (1), ubp15-1 (2), wild type with     UBP15 transgene (3-6) and ubp15-1 with UBP15 transgene (7-9) plants     were analyzed. Total RNA was isolated from rosette leaves grown for     4 weeks. Equal amounts of total RNA from the different plant samples     were used, and gel blot was hybridized and labeled with UBP15     gene-specific probes. The rRNA band pattern was used to show equal     loading. The upper band (upper arrow) was the full length of the     UBP15 mRNA, while the lower band (lower arrow) represented the     truncated mRNA. Lane3, 4 were the samples with UBP15-overexpressing     phenotype while lane 5, 6 were similar to wild type without     obviously UBP15-overexpressing phenotype. Lane 7, 8 but not 9 were     rescued samples for they did not exhibit mutants phenotype but as     normal as wild type. Line 9 sample showed ubp15-1 mutant phenotype. -   (E) RNA gel blot analysis of the UBP15C447A gene expression in     transgenic lines.

FIG. 5. Comparison of wild type and UBP15-overexpressing line.

-   (A) Ninth rosette leaf of wild type. Bar=1 mm. -   (B) Ninth rosette leaf of UBP15-overexpressing line. Bar=1 mm. -   (C) Top view of wild type flower. Bar=1 mm. -   (D) (E) (K) Ectopic flowers of UBP15-overexpressing line. Bar=1 mm. -   (I) Side view of the flower of wild type. Bar=1 mm. -   (J) Side view of the flower of UBP15-overexpressing line. Bar=1 mm. -   (F) Secondary stems of wild type. Bar=1 cm. -   (G) Degenerated secondary stems of UBP15-overexpressing line. Bar=1     cm. -   (H) Siliques of wild type. Bar=1 cm. -   (M) Abnormal siliques of UBP15-overexpressing line. Bar=1 cm. -   (L) Comparison the normal siliques of wild type (left) and     UBP15-overexpressing line (right). Bar=1 cm.

FIG. 6. Comparison of the transverse sections of rosette leaves across the lamina in four lines.

-   (A) From top to the bottom: wild type, ubp15-1, ubp15-2 and     UBP15-overexpressing line. In each panel, two cotyledons and rosette     leaves from the first to the last as well as two first cauline     leaves are placed from left to the right. Arrows indicate positions     of cauline leaves. Bar=1 cm. -   (B) Models demonstrate the position of transverse sections. -   (C) Comparison of adaxial epidermal cell number in transverse     sections across the rosette leaves lamina. Error bars represent     standard deviation of three biological repeats.

FIG. 7. Histological comparison of the transverse sections of the ninth rosette leaf middle region.

-   (A) Comparison of the cell layer in transverse sections of wild     type, ubp15-1, ubp15-2, UBP15-overexpressing line and ubp15 ubp16.     ad, adaxial; pa, palisade; sm, spongy mesophyll; ab, abaxial; x,     xylem; p, phloem. Bar=0.1 mm. -   (B) Comparison of the mid vein structure in transversal sections of     wild type, ubp15-1, ubp15-2, UBP15-overexpressing line and ubp15     ubp16. Bar=0.1 mm.

FIG. 8. Real-time PCR confirm the microarray results.

7 down regulated genes and 2 up regulated genes are randomly picked for real-time PCR analysis which confirms microarray result.

FIG. 9. Characterization of the UBP16 and UBP17.

-   (A) Gene structure of UBP16 (left) and UBP17 (right). -   (B) 12-d-old seedlings of wild type, ubp15-1, ubp15 ubp17, ubp15     ubp16 and ubp15 ubp16 ubp17. Bar=1 cm. -   (C) 2-month-old plants of wild type, ubp15-1, ubp15 ubp17, ubp15     ubp16 and ubp15 ubp16 ubp17. Bar=1 cm.

FIG. 10. Characterization of the UBP18 and UBP19.

-   (A) Gene structure of UBP18 (up panel) and UBP19 (bottom panel). -   (B) ubp19 exhibits recessive embryo lethality. The upper silique is     ubp19 Heterzygote and the lower is wild type. Arrows refer to those     abnormal homozygote embryos. Bar=1 mm. -   (C) Microscopic examination of embryos of wild type (left) and ubp19     homozygote (right). ubp19 homozygote stagnates developing at global     stage. Bar=20 μm.

FIG. 11. Tissue expression pattern of UBP19. The expression pattern of UBP19 was determined using P_(UBP19):GUS transgenic lines.

-   (A) 12-d-old seedling of the P_(UBP19):GUS line. Bar=1 mm. Figure in     the right bottom is 6 fold enlarged of the root tip region. -   (B) Mature rosette leaf of the P_(UBP19):GUS line. Bar=1 mm. -   (C) Inflorescence of the P_(UBP19):GUS line. Figure in the left     bottom is 2 fold of a flower. Bar=1 mm. -   (D) Silique of the P_(UBP19):GUS line. Bar=1 mm.

TABLE 1 Analysis of T-DNA insertion lines for UBP genes. Arabidopsis Genome ID Protein Mutant allele T-DNA line Insertion site Phenotype At2g32780 UBP1 ubp1-2 SALK_086190 Promoter ND At1g04860 UBP2 ubp2-2 SALK_064103 1^(st) exon ND ubp2-3 SALK_059858 1^(st) exon ND At4g39910 UBP3 ubp3-1 SALK_112950 3^(rd) exon ND At2g22310 UBP4 ubp4-1 SALK_043210 4^(th) exon ND At2g40930 UBP5 ubp5-1 SALK_08839 5′UTR ND At1g51710 UBP6 ubp6-1 SALK_108832 14^(th) intron ND At3g21280 UBP7 ubp7-1 SALK_014223 ND ND At5g22030 UBP8 ubp8-1 SALK_034744 5^(th) intron ND ubp8-2 SALK_149329 6^(th) intron ND ubp8-3 SALK_088692 7^(th) exon ND At4g10570 UBP9 ubp9-1 SALK_141485 5′UTR ND At4g10590 UBP10 ubp10-1 SALK_093503 9^(th) exon ND At1g32850 UBP11 ubp11-1 SALK_043515 8^(th) intron ND At5g06600 UBP12 NONE At3g11910 UBP13 ubp13-1 SALK_128312 5^(th) exon ND ubp13-2 SALK_024054 6^(th) exon ND ubp13-3 SALK_130784 17^(th) exon ND ubp13-4 SALK_132368 21^(th) intron ND At3g20630 UBP14 ubp14-3 SALK_050151 9^(th) exon Recessive embryo lethal ubp14-4 SALK_012863 19^(th) exon Recessive embryo lethal At1g17110 UBP15 ubp15-1 SALK_018601 12^(th) exon Recessive rosette leaves narrow and serrated ubp15-2 SALK_015611 8^(th) exon Recessive rosette leaves narrow and serrated At4g24560 UBP16 ubp16-1 SALK_023552 5^(th) exon ND At5g65450 UBP17 ubp17-1 SALK_087726 9^(th) exon ND ubp17-2 SALK_113300 12^(th) exon ND ubp17-3 SALK_009641 8^(th) intron ND At4g31670 UBP18 ubp18-1 SALK_101685 2^(nd) intron ND ubp18-2 SALK_126252 4^(th) exon ND At2g24640 UBP19 ubp19-1 SALK_084566 5′ UTR Recessive embryo lethal ubp19-2 SALK_117787 5′ UTR ND At4g17890 UBP20 NONE At5g46740 UBP21 ubp21-1 SALK_079015 1^(st) exon ND At5g10790 UBP22 NONE At5g57990 UBP23 ubp23-1 SALK_121772 10^(th) exon ND At4g30890 UBP24 ubp24-1 SALK_001531 3^(rd) exon ND At3g14400 UBP25 ubp25-1 SALK_088458 5′ UTR ND ubp25-2 SALK_111336 2^(nd) exon ND At3g49600 UBP26 ubp26-1 SALK_024392 4^(th) intron ND At4g39370 UBP27 ubp27-1 SALK_067020 5′ UTR ND ubp27-2 SALK_027968 1^(st) exon ND 38 T-DNA knockout lines corresponding to the 24 out of 27 UBP genes are screened for their phenotype. Only 5 lines belong to 3 genes exhibit observable phenotype.

TABLE 2 Morphometric analysis of wild type, ubp15-1 mutant, and UBP15 over-expressing plants. UBP15 over-expressing Body parameters Wild type ubp15-1 plants Number of rosette leaves 12.58 ± 0.95 (n = 26) 10.82 ± 1.36 (n = 18) 16.21 ± 1.63 (n = 26) (LD)^(a) Flowering time (LD) (day)^(a) 41.54 ± 3.79 (n = 26) 39.13 ± 2.02 (n = 46) 46.07 ± 2.37 (n = 26) Number of rosette leaves 15.92 ± 2.11 (n = 7) 13.08 ± 1.77 (n = 7) 20.22 ± 2.66 (n = 7) (SD)^(b) Flowering time (SD) (day)^(b) 69.04 ± 1.41 (n = 8) 65.69 ± 4.66 (n = 21) 75.45 ± 4.87 (n = 8) Fresh weight of the rosette 13.24 ± 0.48 (n = 24) 10.74 ± 0.29 (n = 40)  15.6 ± 0.46 (n = 24) leaves (mg/cm²)^(b) Silique length (cm)^(c)  1.36 ± 0.08 (n = 50)  1.09 ± 0.08 (n = 50)  1.42 ± 0.07(n = 40) Root length (cm)^(d)  5.87 ± 0.75 (n = 22)  4.64 ± 0.74 (n = 22)  6.84 ± 0.69 (n = 26) Primary stem length (cm)^(c) 26.09 ± 2.68 (n = 11) 23.77 ± 2.98 (n = 15) 29.25 ± 4.44 (n = 6) Primary stem diameter (mm)^(c)  0.80 ± 0.08 (n = 14)  0.65 ± 0.09 (n = 18)  0.98 ± 0.07 (n = 8) ^(a)Measurements were taken from bolting plants. Plants grow in 16 h light/8 h dark. ^(b)Measurements were taken from bolting plants. Plants grow in 8 h light/16 h dark. ^(c)Measurements were taken from plants 60 d after sowing. Plants grow in 16 h light/8 h dark. ^(d)Measurements were taken from plant 14 d after sowing. Plants grow in 16 h light/8 h dark.

TABLE 3 Microarray Data for Selected Genes with Various Functions Fold Gene Description and Putative AGI Code Change Function GO Category Proteins related to cell cycle At2g23430 1.72 ICK1 Negative regulation of cell division and promoter of endoreduplication. At1g77880 0.3 Cyclin-like F box domain containing protein Proteins regulating flowering At1g26310 1.98 Floral homeotic gene CAL Positive regulation of flower development At5g65080 0.31 MAF5 Negative regulation of flower development, vernalization response Transcription factors At1g74080 4.26 MYB122 Encodes a putative transcription factor At3g07650 2.39 CONSTANS gene family Negative regulation of long-day photoperiodism, flowering At4g17980 2.32 No apical meristem (NAM) Transcription factor activity family protein At3g20810 2.05 jmjC domain-containing Transcription factor activity transcription factor At3g23250 2.03 MYB15 Transcription factor activity, response to kinds of hormone At1g21910 1.92 ERF/AP2 transcription factor Transcription factor activity, TINY-like protein At2g31220 1.86 Basic helix-loop-helix (bHLH) Transcription factor activity family protein At2g19810 0.56 Zinc finger (CCCH-type) family Transcription factor activity protein At5g57660 0.51 B-box type zinc finger family Transcription factor activity protein At1g71030 0.42 MYB family transcription factor Transcription factor activity, response to kinds of hormone, mainly in leaves. At4g16780 0.42 Homeobox-leucine zipper Transcription factor activity, response to protein 4 cytokinin stimulus At3g04070 0.45 No apical meristem (NAM) Transcription factor activity family protein Biosynthetic metabolism At5g38710 4.81 Proline oxidase Glutamate biosynthesis, proline catabolic process, located in MT At4g21990 3.31 APS REDUCTASE 3 Sulfate assimilation, located in chloroplast At3g12430 3.24 3′-5′ exonuclease Nucleic binding, 3′-5′ exonuclease activity At5g06290 2.53 2-cys peroxiredoxin Located in chloroplast, antioxidant activity At3g24420 2.48 Hydrolase, alpha/beta fold family Located in endomembrane system protein At5g61440 2.04 Thioredoxin family protein Thiol-disulfide exchange intermediate activity, located in chloroplast At1g51760 1.96 IAA-amino acid hydrolase 3 IAA-Ala conjugate hydrolase activity At1g76130 1.92 Alpha-amylase Carbohydrate metabolic process, located in extracellular region At4g19170 0.54 Putative nine-cis- Located in plastoglobule epoxycarotenoid dioxygenase At5g35970 0.48 DNA helicase-like DNA-binding protein, located in chloroplast At1g73480 0.47 Alpha/beta fold family hydrolase Aromatic compound metabolism, located in chloroplast At1g77760 0.47 Nitrate reductase 1 (NR1) At3g49160 0.43 Pyruvate kinase-like protein Pyruvate kinase activity, involved in glycolysis At1g77760 0.43 Nitrate reductase Response to light stimulus, nitric oxide biosynthetic process At5g24470 0.42 APRR5 Circadian rhythm, photomorphogenesis At5g11330 0.41 Monooxygenase family protein Electron transport, metabolic process, Located in endomembrane system At1g32900 0.39 Starch synthase Transferase activity, transferring glycosyl groups, located in chloroplast At5g48490 0.28 Lipid transfer protein (LTP) Lipid binding and transport, located in family protein endomembrane system Polysaccharide metabolism At5g25980 4.53 Glycosyl hydrolase family 1 Hydrolase activity, hydrolyzing O-glycosyl compounds At1g55850 3.57 Cellulose synthase family Polysaccharide biosynthetic process, cell wall protein biosynthetic process At3g44990 2.52 Xyloglucan: xyloglucosyl Hydrolase activity, acting on glycosyl bonds, transferase located in chloroplast At2g32290 2.3 Putative 1,4-alpha-D-glucan Polysaccharide catabolic process maltohydrolase At3g21750 2.17 UDP-glucosyl transferase family Transferring glycosyl groups protein Signal transduction At5g39670 3.03 Calcium-binding EF hand family protein At1g14320 2.52 Wilm's tumor suppressor Involved in translation protein-related At5g35735 2.04 Auxin-responsive family protein Dopamine beta-monooxygenase activity, located in membrane At1g61370 2.1 S-locus lectin protein kinase Protein amino acid phosphorylation, located in family protein endomembrane system At1g51760 1.96 IAA amino acid hydrolase (IAR3) Proteolysis, located in endomembrane system At5g67030 0.55 Zeaxanthin epoxidase Abscisic acid biosynthetic process At5g45830 0.52 Tumor-related protein like At4g12980 0.51 Auxin-responsive family Dopamine beta-monooxygenase activity, protein, putative located in membrane At4g28950 0.47 ROP GTPase gene family Protein transport, small GTPase mediated protein signal transduction At5g45820 0.26 CBL-interacting protein kinase Kinase activity 20 (CIPK20) Photosynthesis At3g17040 0.5 Tetratricopeptide repeat (TPR)- Chloroplast precursor containing protein At3g59400 0.37 GUN4 Chlorophyll biosynthetic process, located in chloroplast At1g44446 0.34 Chlorophyll a oxygenase/ Chlorophyll biosynthetic process chlorophyll b synthase

FIG. 12. Alignment of 27 UBP proteins.

Highly conserved amino acids are shaded in black while less conserved ones are shaded in gray. Numbers above the alignment indicate the amino acid position in the consensus.

FIG. 13. Gene expression pattern of UBP15 subfamily.

Organs from 1 to 18 are cauline leaves, rosette leaves, pistil one day before pollination, pistil one day after pollination, silique 3 day after pollination, silique 8 day after pollination, stem, sepal, stamen, petal, seed, cultured cell, root dark, root white light, hypocotyl dark, hypocotyl white light, cotyledon dark and cotyledon white light.

FIG. 14. Phylogenetic Analysis of AtUBP15 subfamily and its homologues in Rice.

The Phylogenetic tree of 9 UBPs in Arabidopsis or Rice. Bootstrap values are shown in percentages at nodes.

FIG. 15. Two month old lines of wild type, two ubp15 mutants and UBP15-overexpressing line.

Two-month-old wild type, ubp15-1, ubp15-2, UBP15-overexpressing line and rescued line. Mutants are weak, with early flowering time and more secondary stems while UBP15-overexpressing line showed opposite phenotype with late flower and strong apical dominance. Bar=1 cm.

FIG. 16. Comparison of palisade cell number in transverse sections across the lamina of rosette leaf. Error bars represent standard deviation of three biological repeats.

FIG. 17. Comparison of the ninth rosette leaf of wild type and mutants as well as transgenic lines.

-   (A) Mature ninth rosette leaf of wild type, ubp15-1, ubp15-2,     UBP15-overexpressing line and ubp15 ubp16. Bar=1 cm. -   (B) Comparison of adaxial epidermal cell numbers of transverse     sections in three regions of the ninth rosette leaf.

SUPPLEMENTAL TABLES

SUPPLEMENTAL TABLE 1 Microarray data of 27 UBP genes expression in various organs. Pistil one Pistil one Silique 3 day Silique 8 day Gene gene day after day before after after code name Cauline leaf Rosette leaf pollenation pollenation pollenation pollenation At4g10590 UBP10 253.2371134 538 318.9969539 178.5757576 209.7058824 69 At4g10570 UBP9 253.2371134 538 318.9969539 178.5757576 209.7058824 69 At1g32850 UBP11 14.17808219 19 10.58646617 12.07272727 38.05147059 14.80555556 At2g40930 UBP5 114.5257732 497.5804196 350.327381 404.625 337.3897059 70 At5g22030 UBP8 123.0618557 309.4912281 218.0594178 315.5220588 311 89.97222222 At4g30890 UBP24 248 584.2237762 655.5600733 568 736.5073529 168.5555556 At4g39910 UBP3 172.9726027 350.6993007 302.4974359 372.8897059 208.8602941 130.9722222 At2g22310 UBP4 38.41237113 66.24561404 63.11683054 48 28 22 At5g06600 UBP12 1141 1519.146853 1139.097744 599.6121212 1186.024096 247.1388889 At3g49600 UBP26 190 480.2807018 330.575188 343.5955882 313.1325301 219 At1g51710 UBP6 621 1231.754386 891.3714671 781.1764706 754.2647059 574 At3g21280 UBP7 71 292.9370629 145.1863505 160.5073529 136.1397059 107 At2g32780 UBP1 7 8.251748252 51.91666667 29.67878788 15.22058824 35 At1g04860 UBP2 211.2680412 381.2307692 367.7518797 222.8424242 306.9485294 149 At4g39370 UBP27 46.94845361 74.52631579 127.5 61.02941176 57 77.9 At5g10790 UBP22 379.1443299 600.3508772 273.7743975 238.0147059 289.1911765 91 At5g46740 UBP21 120.9278351 158.4335664 383.9718913 241.4545455 222.3897059 124.1388889 At5g57990 UBP23 491 1614.736842 1162.335897 1227.911765 1056 726.6111111 At3g14400 UBP25 407.5979381 719.3859649 611.4935415 376.2666667 496.0240964 315.4722222 At4g24560 UBP16 152.2268041 443.9440559 509.277381 546.8235294 367.1686747 142.3611111 At5g65450 UBP17 59.04123711 193.0909091 134.8794872 150.9090909 152.2058824 85 At1g17110 UBP15 711.3402062 1031.982456 1031.665293 758.0666667 845 514.7777778 At4g31670 UBP18 142 404.3356643 203.3615577 209.3308824 181.8014706 188 At2g24640 UBP19 56 222 205.9252747 238.0147059 203 84.27777778 Gene gene code name Stem Sepal Stamen Petal Seed Cultured cell At4g10590 UBP10 266 504.8139535 661.641791 290 95.75543478 963.8555417 At4g10570 UBP9 266 504.8139535 661.641791 290 95.75543478 963.8555417 At1g32850 UBP11 52 91.84883721 64.74129353 134 −3.02173913 34.26132223 At2g40930 UBP5 315.9270073 246.3023256 270 798 67.02173913 1217.020979 At5g22030 UBP8 444 29.51162791 451.2704918 886.7755102 116.8865489 417.7322314 At4g30890 UBP24 646.8076923 562.5348837 707 1767.030612 191.9293478 1559.865613 At4g39910 UBP3 524.2627737 458.3953488 750.5721393 1617 68.875 1084.045697 At2g22310 UBP4 143.0192308 90.53488372 101 160 −10.30366848 65.2861244 At5g06600 UBP12 1903.386861 204.5813953 1246 2006 401.0923913 2426.601399 At3g49600 UBP26 551.4615385 195.755814 215.6721311 465.122449 213.3043478 560.5384615 At1g51710 UBP6 1669.846154 406.5465116 901 1469 394.9476902 6227.830303 At3g21280 UBP7 263.1094891 138.7674419 125 294.505102 71.46195652 274.6139657 At2g32780 UBP1 21 67.65116279 39.12935323 118 30.04415761 28.70312881 At1g04860 UBP2 324 590.1046512 639.5870647 256.4693878 261.9293478 819.7538462 At4g39370 UBP27 43 114.4302326 122.3681592 116 248.3913043 64.60289855 At5g10790 UBP22 289 409.6046512 407 834 139.798913 371.109589 At5g46740 UBP21 243.5192308 135.1860465 118.0995025 146.7091837 72.24456522 93.65178979 At5g57990 UBP23 2079.445255 431.5581395 346 929.1581633 534.28125 3446.150487 At3g14400 UBP25 697.0576923 277.3837209 758 214.0867347 207.9673913 1548.92372 At4g24560 UBP16 351.75 318.744186 454 542 93.54076087 1062.276923 At5g65450 UBP17 98.78832117 178.4767442 108.8507463 455 276.5108696 88.66155158 At1g17110 UBP15 851.6730769 379.5930233 534.2935323 207.5663265 210.125 641.6596737 At4g31670 UBP18 398.0875912 309.0348837 322 880 130.9728261 574.4164103 At2g24640 UBP19 331 172.5348837 269.6368159 547.7142857 112.7391304 556.7737557 Gene gene Root white Hypocotyl Hypocotyl Cotyledon Cotyledon code name Root dark light dark white light dark white light At4g10590 UBP10 424.8228346 438.28125 173.40625 131.5095238 393.2027027 370.7176157 At4g10570 UBP9 424.8228346 438.28125 173.40625 131.5095238 393.2027027 370.7176157 At1g32850 UBP11 51.77382175 85.8125 17.91666667 36.67142857 44.11560694 39.55357143 At2g40930 UBP5 325.4406923 344.65625 97.63541667 123.1904762 353.9322034 313.0154762 At5g22030 UBP8 279.9637111 408.21875 129.2604167 143.8857143 419.0860927 422.2265816 At4g30890 UBP24 414.0984252 531.8125 188.71875 313.3857143 467.1186441 429.1309524 At4g39910 UBP3 462.4347826 666.46875 311.2708333 294.1071429 540.1788079 598.1203056 At2g22310 UBP4 128.5507246 111.09375 20.54166667 46.95714286 62.12582781 101.2047619 At5g06600 UBP12 1517.831793 2085.65625 416.6458333 406.9738095 1479 1652.075033 At3g49600 UBP26 425.0354331 616.53125 202.71875 183.6095238 397.9595376 378.8214286 At1g51710 UBP6 1981.102362 3926.3125 569.9583333 668.4071429 889 1159.790698 At3g21280 UBP7 105.6540784 209.125 42.21875 91.56428571 131.4277457 177.4428571 At2g32780 UBP1 62.84468789 34.8125 20.13541667 28.72619048 26.65317919 26.14784053 At1g04860 UBP2 502.2960018 594.59375 183.71875 200.4095238 438.0397351 410.7517483 At4g39370 UBP27 92.94123017 106.28125 28.96875 47.19047619 109 73.32009044 At5g10790 UBP22 410.9566929 420.59375 106.6354167 127.0714286 470.7118644 562.8515873 At5g46740 UBP21 146.8093119 215.71875 63.33333333 84.58809524 145.2138728 122.7753913 At5g57990 UBP23 832.6963369 1380.65625 540.7708333 948.9547619 817.1125828 1300.761526 At3g14400 UBP25 730.0184868 1210.8125 323.5520833 322.2595238 837.2774566 704.6364653 At4g24560 UBP16 345.6990291 359.90625 148.8854167 179.4928571 431.9653179 379.5714286 At5g65450 UBP17 171.0468619 137.28125 48.69791667 90.40714286 195.8543046 184.5927003 At1g17110 UBP15 787.4924113 1596.84375 409.7291667 498.3833333 1680.243243 1613.125 At4g31670 UBP18 388.7701246 783.5625 268.8229167 230.0404762 196.7288136 236.5464286 At2g24640 UBP19 216.5870136 405.65625 110.78125 162.3714286 315.8513514 298.2021164

SUPPLEMENTAL TABLE 2 Primers designed to identify  the genotype of T-DNA insertion lines. T-DNA insertion Forward (FP) and lines reverse (RP) primers SALK_086190 FP: 5′-TGCGTGAAGGAATTCAGATCCA-3′ RP: 5′-TTCAGCGTTATATCTAAAAGAATTG-3′ SALK_064103 FP: 5′-GCTTCGCTTACGTTATACCACGC-3′ RP: 5′-CTGAAGCCTCGGGAGTTGGTT-3′ SALK_059858 FP: 5′-CGGGTCTTCTCCGCTACACCT-3′ RP: 5′-CCTTTGGTGGTTGCAGATTCG-3′ SALK_112950 FP: 5′-TGTGCACAACACCATTTGCCT-3′ RP: 5′-TCTCTCCCTTGTGCAGGCTCTT-3′ SALK_043210 FP: 5′-TGTGATTGGGTTTGGTTTGGG-3′ RP: 5′-TCTCTTGACCTGCTTGGCTGA-3′ SALK_088398 FP: 5′-GTGCTGCTACTGCTGCTTCCC-3′ RP: 5′-CAACAGCAGCTAAATCAAAAAGG-3′ SALK_108832 FP: 5′-AAAATGTGGTCCAAGTGGATGG-3′ RP: 5′-TGAGAAGGAAACTCACATGACTGGA-3′ SALK_014223 FP: 5′-CCAATTACAGTGCGTTCCAAGC-3′ RP: 5′-TGGCCAACTTTGTTAGATGTTTCA-3′ SALK_034744 FP: 5′-GACCAAGGGGATTCCAAATGC-3′ RP: 5′-TTTCTGGTTGCAGGGCCAATA-3′ SALK_149329 FP: 5′-AGCGGGAAATCCACATATGCC-3′ RP: 5′-CCTTTCCAATGGTTTTCAGGC-3′ SALK_088692 FP: 5′-CGTAAGCAGCCGAGGTCTTGA-3′ RP: 5′-TCCAAGCGGTTGAATGTGCTT-3′ SALK_141485 FP: 5′-TGCAATGATGCTAATTGGATCAAGA-3′ RP: 5′-TTTTATTATGCTTCTGTTCCTTTTT-3′ SALK_093503 FP: 5′-AGCATCAGGAAGGTGGCCATT-3′ RP: 5′-TCGGTTACCATTTCCTTCCATTG-3′ SALK_043515 FP: 5′-CACTAGGAAACCAGTGCCTTCG-3′ RP: 5′-ACACTTTGGGCCCCTGTCACT-3′ SALK_128312 FP: 5′-CCCTCCACAACAGTTCCCTTG-3′ RP: 5′-TTGGAATGGAGTCAAGTTACCGC-3′ SALK_024054 FP: 5′-CGCACTATGAACCCCAACACC-3′ RP: 5′-GAAAGGTTGGATGCTTGTTTTG-3′ SALK_130784 FP: 5′-GCTTTTGTTGGAACAGATGTCAA-3′ RP: 5′-TCCTCATGTAGGAAGAGGTAGCCA-3′ SALK_132368 FP: 5′-CCAAGCTTCTCAGCCACCCTT-3′ RP: 5′-TGTTGGCAGGCTAATGGTGAAA-3′ SALK_050151 FP: 5′-GCCGAAAAGGAGTATCGTTCCA-3′ RP: 5′-CAAGGTAGATGCCATTGCCCA-3′ SALK_012863 FP: 5′-GGAGGCAAATTAAAAAGACAGCGA-3′ RP: 5′-ATGCACCAATCTCCCACCAGA-3′ SALK_018601 FP: 5′-ATGGTGAACCGGAGCTTTTCC-3′ RP: 5′-CCAGGTTAAATGCCTGAGGTGTG-3′ SALK_015611 FP: 5′-TCACACCTCAGGCATTTAACC-3′ RP: 5′-TTGTGGAAACAGGTATTGTCTC-3′ SALK_023552 FP: 5′-TACGCAAATGAAAGACCATGA-3′ RP: 5′-TGGGTTTGAGAAGCTGGTCGT-3′ SALK_087726 FP: 5′-GGTGAATCATATGGGTTTTGCTTT-3′ RP: 5′-TTTGAACCAATCTCCATCAAGGG-3′ SALK_113300 FP: 5′-TGCTTCTTTATGCAAGGTGAATGA-3′ RP: 5′-CATACTCCCTCCGTTTTCACAA-3′ SALK_009641 FP: 5′-AAAGGCAAGGGGAGGAGAATC-3′ RP: 5′-GAAGCTCGGGAAAATGGATGG-3′ SALK_101685 FP: 5′-TGAGCATCCTCCTGTCTTCCA-3′ RP: 5′-TTTTTCACATTGTTACCCAAAAA-3′ SALK_126252 FP: 5′-TGAGCATCCTCCTGTCTTCCA-3′ RP: 5′-TTTTTCACATTGTTACCCAAAAA-3′ SALK_084566 FP: 5′-TCGGCGATGGTCTCTATCGAA-3′ RP: 5′-GGTTGATAACAATTTACCAAAGTCG-3′ SALK_117787 FP: 5′-TGCGTGAAGGAATTCAGATCCA-3′ RP: 5′-TTCAGCGTTATATCTAAAAGAATTG-3′ SALK_079015 FP: 5′-TTTAAGTTTTCTAGACACTATTTTT-3′ RP: 5′-GGGAGAAAGCCGAGAGTCTGTG-3′ SALK_121772 FP: 5′-TGTAACCTCGATCCCTCAGCATC-3′ RP: 5′-TTGCCAAATGGGATGAGGAAA-3′ SALK_001531 FP: 5′-CCTTCCCAGTAACCGAGGCTCT-3′ RP: 5′-CCTTTTGTGCAGCTCCTCCAG-3′ SALK_088458 FP: 5′-CGGAGAAAACCAACCAAGCAA-3′ RP: 5′-ACAGCTATTGCCGGTGTAGCG-3′ SALK_111336 FP: 5′-TGAACGTTGCAAATTCATTCGAT-3′ RP: 5′-CCGATGCGCCTAACAAGATTTC-3′ SALK_024392 FP: 5′-TTGTGGAAACACCCCACAAAA-3′ RP: 5′-TTGGCTTCGTCTATGGGCTGA-3′ SALK_067020 FP: 5′-TTCTCAAAACATTCGCAGTGGC-3′ RP: 5′-AATAGACCGTGCTGTTGGGCA-3′ SALK_027968 FP: 5′-TTTCAAATCAAATAAGCTAAAAAG-3′ RP: 5′-TGGCTTGTCAAATTGAAATTTTTG-3′

SUPPLEMENTAL TABLE 3 Transcriptome analysis of ubp15-1. Gene Code ID M W M/W At1g17110 AF302665 110 1959 0.06 At1g28375 AC010155 21 221 0.09 At4g01525 AC069551 25 236 0.11 At1g14550 AC010657 32 204 0.16 At3g59970 AF181966 39 239 0.16 At5g05820.a F15569 45 270 0.17 At3g29000 AB025615 37 209 0.18 At4g12900 AL079349 47 247 0.19 At1g38450 AC006918 50 233 0.22 At1g41720 AC006918 50 233 0.22 At2g06330 AC006918 50 233 0.22 At1g42360 AC006918 50 233 0.22 At1g42370 AC006918 50 233 0.22 At1g37160 AC006918 50 233 0.22 At5g39890 AB010077 57 256 0.22 At1g63530 AC008047 56 253 0.22 At1g71150 AC016972 55 244 0.22 At1g32060 AC074309 517 2159 0.24 At5g66990 AB026640 73 302 0.24 At1g35690 AC007887 81 322 0.25 At5g41315 AB006707 60 230 0.26 At3g02120 AC011664 76 290 0.26 At4g02240 AL096882 64 244 0.26 At5g65330 AL096882 64 244 0.26 At5g45820 AB016870 495 1874 0.26 At2g06410 AC006918 69 244 0.28 At5g48490 AB020745 2248 7953 0.28 At4g28440 AV557403 62 217 0.29 At1g62710 AF367254 85 281 0.3 At1g77880 AC009243 83 276 0.3 At1g48980 AC016041 61 203 0.3 At3g60500 AL138646 62 206 0.3 At3g01650 AC009325 71 241 0.3 At5g01600 AF326869 5374 17383 0.31 At5g16580 AB008270 72 231 0.31 At1g14500 AC012188 71 228 0.31 At5g65080 AF214485 114 363 0.31 At4g07938 AC006423 63 200 0.31 At5g02720 AL162973 66 212 0.31 At5g58830 AB016885 120 386 0.31 At1g43830 AC006423 63 200 0.31 At2g38690 AC005499 90 287 0.31 At2g02690 AC002521 64 201 0.32 At1g51960 AC006216 160 502 0.32 At1g48660 AC073555 116 364 0.32 At5g19840 AB024038 71 218 0.33 At1g65920 AC009513 123 376 0.33 At4g24080 AC002343 94 282 0.33 At3g55240 AL132954 508 1545 0.33 At1g44446 AB021316 3029 8868 0.34 At4g39090 AL035679 2180 6320 0.34 At4g38590 AL035540 74 220 0.34 At4g12440 AL049730 80 231 0.34 At4g20450 AL080253 104 308 0.34 At2g29670 AF375460 6906 19504 0.35 At4g31360 AL021633 190 547 0.35 At1g53930 AC006577 112 318 0.35 At3g63160 BE039458 1963 5579 0.35 At2g34940 AC004238 113 320 0.35 At3g26210 AB024038 515 1421 0.36 At5g44510 AB017065 73 202 0.36 At1g32810 AC006424 153 421 0.36 At4g13490.a AA404812 4980 13728 0.36 At3g58650 AL137082 87 244 0.36 At5g62080 AB016880 81 217 0.37 At4g09930 AL049481 110 297 0.37 At1g47730 AC007519 110 296 0.37 At2g22240 U30250 235 626 0.37 At3g59400 AL356014 6379 17232 0.37 At3g01080 AC008261 102 276 0.37 At2g46590 AC006418 145 386 0.38 At4g20970 AL080282 95 248 0.39 At3g27500 AB025626 78 200 0.39 At1g17740 AB010407 105 267 0.39 At4g26460 AL022223 100 256 0.39 At5g54190 U29699 880 2255 0.39 At3g56790 AL390921 111 287 0.39 At3g46760 AL096859 80 207 0.39 At1g32900 AC006424 158 406 0.39 At5g49140 AB023028 107 268 0.4 At4g36195 AL022141 97 242 0.4 At4g35960 AL022373 96 242 0.4 At3g30130 AY046045 221 555 0.4 At1g74980 AY045856 476 1195 0.4 At1g77410 AC078898 85 214 0.4 At1g49800 AC079674 112 280 0.4 At1g28470 AV567286 152 381 0.4 At1g56350 AY046045 221 555 0.4 At2g18150 AC007212 152 383 0.4 At1g05700 AC007153 108 273 0.4 At4g29230 AL161574 126 313 0.4 At3g52040 AL049711 94 236 0.4 At1g63570 AC008047 151 378 0.4 At5g11330 AL360314 1143 2805 0.41 At3g13760 AP001307 151 368 0.41 At1g27220 AC004557 85 207 0.41 At1g04710 AC002376 144 356 0.41 At5g51670 AB025607 198 477 0.41 At1g63840 H77052 242 585 0.41 At2g31670 AV540982 214 519 0.41 At4g20380 U87834 101 247 0.41 At3g18780 U41998 687 1650 0.42 At3g03590 AC009327 190 450 0.42 At3g27160 AY039901 6880 16566 0.42 At4g16780 X68146 1165 2800 0.42 At1g56080 AC009894 115 272 0.42 At3g25080 AB026647 163 389 0.42 At3g10440 AC011560 231 555 0.42 At2g11010 AB028615 133 315 0.42 At2g46570 AC006418 84 200 0.42 At1g71030 Z68157 3598 8496 0.42 At1g41630 AC006250 238 572 0.42 At1g41600 AC006250 238 572 0.42 At1g41660 AC006250 238 572 0.42 At4g23700 AL035394 142 336 0.42 At4g10220 AF096373 89 211 0.42 At5g37230 AB017069 104 245 0.42 At5g37250 AB017069 104 245 0.42 At5g37270 AB017069 104 245 0.42 At5g03350 AL162751 2212 5268 0.42 At5g24470 AF027408 407 972 0.42 At1g79910 AC011717 104 247 0.42 At1g62690 AC007190 137 317 0.43 At5g06980 AY042849 657 1544 0.43 At1g75100 AC013258 117 271 0.43 At1g30080 AC022455 108 251 0.43 At2g35310 AC004667 171 397 0.43 At1g44542 AC084807 133 312 0.43 At1g50720 AC079027 120 276 0.43 At2g47150 AC004411 103 238 0.43 At2g46140 AC005397 112 259 0.43 At3g51150 AL132980 93 218 0.43 At3g42230 AL138645 168 390 0.43 At3g49160 AL132956 485 1128 0.43 At4g36470 AL161589 146 340 0.43 At1g36960 AC051631 86 202 0.43 At1g66100 AF380652 6908 15905 0.43 At2g47860 AC005309 117 275 0.43 At3g60570 AL138646 116 260 0.44 At1g08630 AC003981 93 213 0.44 At3g04360 AC016829 89 201 0.44 At5g26700 AF058914 111 255 0.44 At1g04570 AC002376 117 263 0.44 At2g19070 AC002392 92 206 0.44 At2g04440 AC006951 113 256 0.44 At2g41300 AC005662 107 245 0.44 At4g23970 AL078468 114 254 0.45 At1g43880 AC006423 147 331 0.45 At1g27490 AC004557 116 260 0.45 At1g65300 AC004512 106 236 0.45 At3g04070 AC011698 152 335 0.45 At1g38196 AC006423 147 331 0.45 At3g58350 AL137081 180 401 0.45 At1g80640 AC018849 96 214 0.45 At3g45390 AL132953 115 254 0.45 At1g14390 AC012188 188 407 0.46 At1g37130 AF367272 4767 10361 0.46 At5g51760 AB010074 132 289 0.46 At2g11760 AC074109 217 468 0.46 At2g12010 AC074109 217 468 0.46 At2g34980 AC004238 100 215 0.46 At5g39330 AB009054 171 370 0.46 At4g12210 AL080318 103 224 0.46 At4g12220 AL080318 103 224 0.46 At3g45650 AL138657 239 519 0.46 At5g62130 AB016880 343 745 0.46 At3g59060 AL163527 2960 6497 0.46 At1g38340 AC074109 217 468 0.46 At5g27700 AV534288 124 271 0.46 At1g38149 AC074109 217 468 0.46 At4g07733 AC074109 217 468 0.46 At3g16320 AC001645 119 260 0.46 At1g09150 AC003114 104 227 0.46 At1g20030 AC022472 330 699 0.47 At1g19010 AF360209 217 458 0.47 At2g36050 AY044326 179 381 0.47 At3g48800 AL132963 186 397 0.47 At4g00320 AL161471 202 429 0.47 At3g19050 AP000735 149 315 0.47 At5g46330 AB010698 101 216 0.47 At1g73480 AY045929 1324 2806 0.47 At1g77760 AC012193 1190 2545 0.47 At5g08480 AB006697 120 255 0.47 At3g51830 U72504 886 1904 0.47 At4g28950 AF079484 112 237 0.47 At4g18250 AL021713 116 249 0.47 At3g19700 AP000417 186 400 0.47 At3g48940 AL132967 98 207 0.47 At5g42250 AB023032 935 1961 0.48 At5g35970 AB026643 2449 5056 0.48 At1g06210 AC025290 265 546 0.48 At4g17460 U09332 2470 5158 0.48 At1g44860 AC007264 125 259 0.48 At2g10370 AC007264 125 259 0.48 At1g43740 AC009526 126 262 0.48 At1g43750 AC009526 126 262 0.48 At5g41040 AY034954 221 456 0.48 At5g04950 AB005245 161 338 0.48 At4g35820 AL031986 162 338 0.48 At5g02810 AY039943 2587 5372 0.48 At1g42400 AC007264 125 259 0.48 At2g31900 AC006533 127 261 0.48 At3g02380 AF370149 221 459 0.48 At4g27310 AL030978 621 1281 0.49 At1g76310 AC012394 245 504 0.49 At4g23520 AL031326 121 245 0.49 At3g50900 AL049862 116 238 0.49 At3g15353 AF013959 11215 22738 0.49 At1g12490 AC025416 138 282 0.49 At4g17000 AL161545 195 396 0.49 At2g15730 AC006248 139 283 0.49 At5g16190 AL391148 141 287 0.49 At3g59580 AL138659 145 298 0.49 At3g61190 AL137898 119 243 0.49 At5g53040 AB018116 108 221 0.49 At5g64170 AB008266 736 1512 0.49 At1g13650 AC027656 1432 2937 0.49 At5g10660 AL392144 125 255 0.49 At1g52300 AF370216 3677 7323 0.5 At4g29650 AL079344 247 497 0.5 At1g31300 AI995950 108 214 0.5 At4g29960 AL050352 120 238 0.5 At1g63420 AF372939 221 441 0.5 At1g61220 AV565744 174 352 0.5 At3g26610 X98130 167 337 0.5 At4g38970 AV440437 123 249 0.5 At5g42160 AB017067 129 257 0.5 At3g60380 AL138646 115 230 0.5 At4g36050 AL022373 127 251 0.5 At5g65380 AB011479 545 1080 0.5 At5g03090 AL163002 472 950 0.5 At1g80310 AC018848 740 1489 0.5 At3g17040 AB026636 1749 3490 0.5 At3g44530 AL353818 170 339 0.5 At1g17990 AF344314 1752 3437 0.51 At5g64840 AB019236 3117 6109 0.51 At1g64740 M21414 1506 2968 0.51 At2g43040 AC006224 188 371 0.51 At5g57660 AB018118 6011 11797 0.51 At3g20540 AP000410 219 432 0.51 At5g39865 AB010077 136 268 0.51 At5g17300 AB005238 211 412 0.51 At1g18020 AF344314 1752 3437 0.51 At1g50910 AC079284 261 513 0.51 At5g51440 AB025621 184 363 0.51 At2g06880.a AF147259 117 230 0.51 At3g32020.b AF147259 117 230 0.51 At4g07730.a AF147259 117 230 0.51 At2g03200 AC005313 159 312 0.51 At3g60870 AL162295 234 458 0.51 At3g50800 AL049862 131 259 0.51 At5g41830 AB016871 339 668 0.51 At5g53310 AF361603 583 1145 0.51 At4g12980 AL079349 2345 4580 0.51 At2g30730 AC002340 178 350 0.51 At3g52270 AL132972 135 265 0.51 At3g21080 AP000604 172 336 0.51 At2g30510 AF181683 3085 6075 0.51 NoAnno AA585895 189 364 0.52 At2g34480 AY042803 2958 5666 0.52 At1g06450 AC007592 229 437 0.52 At5g52020 AB015478 104 200 0.52 At1g62060 X91954 145 279 0.52 At2g13690 AC006436 107 205 0.52 At1g20780 AC069251 379 729 0.52 At3g17930 AY039550 1550 2953 0.52 At3g54590 AP002543 190 364 0.52 At4g08410 AP002543 190 364 0.52 At5g06640 AP002543 190 364 0.52 At2g44470 AC004521 114 219 0.52 At1g34740 AC007894 113 219 0.52 At1g52020 AC007894 113 219 0.52 At2g14770 AC007894 113 219 0.52 At3g24390 AC007894 113 219 0.52 At3g42730 AC007894 113 219 0.52 At4g05280 AC007894 113 219 0.52 At5g36860 AC007894 113 219 0.52 At1g21940 AC013482 128 248 0.52 At1g34290 AC007454 110 213 0.52 At1g62000 X91954 145 279 0.52 At1g62080 X91954 145 279 0.52 At3g06020 AC013454 171 328 0.52 At1g17390 AC007843 254 492 0.52 At2g05560 AC007894 113 219 0.52 At1g68850 AC011914 144 276 0.52 At1g73600 AC079676 6072 11568 0.52 At2g05130 AB015477 113 217 0.52 At1g04380 AC000104 119 227 0.52 At4g04710 AB015477 113 217 0.52 At1g25886 AC007894 113 219 0.52 At4g03300 AC007894 113 219 0.52 At4g08880 AC007894 113 219 0.52 At4g08400 AP002543 190 364 0.52 At4g10710 AF080119 208 402 0.52 At3g43990 AB015477 113 217 0.52 At5g34940 AA586196 211 403 0.52 At3g54500 AL138656 183 350 0.52 At3g27560 X92728 167 323 0.52 At5g16030 AL391145 7145 13777 0.52 At3g25960 AB023041 434 835 0.52 At2g16980 AC002354 204 389 0.52 At4g10670 AF080119 208 402 0.52 At1g61500 AC005850 247 475 0.52 At5g45830 AB016870 306 590 0.52 At5g35520 AB015477 113 217 0.52 At3g54860 AL049655 130 247 0.52 At1g31710 AC074360 240 449 0.53 At2g21110 AC006264 117 219 0.53 At5g60390 AF360167 7372 13840 0.53 At5g44220 AB005239 225 423 0.53 At3g57160 AL138655 194 362 0.53 At1g11620 AC007296 128 239 0.53 At4g14450 AF067468 114 213 0.53 At2g42340 AC005956 162 304 0.53 At3g21670 AF372959 748 1399 0.53 At1g54300.a AC005287 174 327 0.53 At2g02850 AC004138 129 246 0.53 At2g26690 AC003105 2529 4731 0.53 At4g17910 AP002057 118 222 0.53 At3g58340 AL137081 131 248 0.53 At4g24480 AL078637 191 362 0.53 At2g29000 AC005315 124 236 0.53 At5g45810 AB016870 272 514 0.53 At2g18000 AC006201 123 233 0.53 At2g25260 AC007070 232 437 0.53 NoAnno AI099709 159 295 0.54 At4g19170 AL021687 1362 2532 0.54 At1g10610 AC007067 221 412 0.54 At5g05690 X87368 2014 3720 0.54 At1g51480 AB026651 186 343 0.54 At5g43730 AB026651 186 343 0.54 At1g37040 AC020646 158 292 0.54 At2g04770 AC020646 158 292 0.54 At2g38320 AF370310 200 371 0.54 At4g37550 AY045895 1113 2075 0.54 At1g49090 AC020646 158 292 0.54 At5g03415 AJ294532 249 458 0.54 At5g16700 AL391147 182 337 0.54 At1g20390 AC027665 185 340 0.54 At1g77150 AV544954 127 236 0.54 At1g77170 AV544954 127 236 0.54 At1g68870 AC011914 438 804 0.54 At3g43210 AL353871 174 326 0.54 At3g05880 AC012393 7580 14042 0.54 At5g20410 AJ000331 111 205 0.54 At2g24430 AC006403 157 292 0.54 At1g26800.a AC006535 155 288 0.54 At1g73660.a BE037745 371 684 0.54 At1g64860 AB004821 2996 5515 0.54 At5g34810 AL161499 222 411 0.54 At5g30480 AC020646 158 292 0.54 At3g01120 AF039206 227 417 0.54 At5g53260 AB013388 128 236 0.54 At4g04130 AL161499 222 411 0.54 At5g62780 AB009053 150 278 0.54 At3g22060 AY034900 1041 1922 0.54 At1g62070 AC000375 336 620 0.54 At1g06570 AF000228 713 1301 0.55 At4g01740 AL161492 182 333 0.55 At5g18620 U95990 188 344 0.55 At3g26190 AB024038 218 394 0.55 At3g61580 AJ224161 139 250 0.55 At4g12010 AL049638 199 360 0.55 At2g37640 AC004684 134 245 0.55 At1g26390 AC013427 174 317 0.55 At1g26400 AC013427 174 317 0.55 At1g26420 AC013427 174 317 0.55 At2g28440 AC006283 190 345 0.55 At4g18110 AL110123 143 262 0.55 At1g70260 AC002062 176 319 0.55 At1g58310 AC008051 117 212 0.55 At3g13229 AB024034 190 345 0.55 At3g12440 AC069474 145 263 0.55 At3g31930 AP001301 217 394 0.55 At2g20740 AC006234 150 272 0.55 At1g26810 AC006535 166 302 0.55 At1g47790 AC012463 302 545 0.55 At1g47560 AC007519 149 273 0.55 At4g14790.a AJ132843 250 453 0.55 At3g62260 AL138651 180 327 0.55 At3g32091 BE521910 134 244 0.55 At3g44720 AC002534 126 227 0.55 At2g34320 AC004481 156 284 0.55 At4g34840 AL079347 109 201 0.55 At3g61750 AL132959 176 318 0.55 At5g39530 AA395409 5835 10560 0.55 At5g26840 AL132976 5258 9555 0.55 At2g23330 AC002391 284 519 0.55 At2g11680 AC007187 165 298 0.55 At3g54210 AL132957 5028 9190 0.55 At5g49050 AB017061 151 273 0.55 At5g67030 AB030296 3968 7179 0.55 At1g28300 AC021044 127 229 0.56 At1g07180 AC067971 774 1388 0.56 At2g28580 AC007171 178 319 0.56 At5g16440 AF188067 218 390 0.56 At2g19810 AC005169 516 927 0.56 At5g44690 AB016874 140 251 0.56 At4g17720 AL161547 639 1148 0.56 At5g10220 AY014798 487 272 1.79 At4g20990 AL080282 306 171 1.79 At4g12290 AL080318 1516 845 1.79 At3g04640 AC011437 1081 604 1.79 At3g19280 AP000419 835 465 1.79 At1g11170 AC007259 370 207 1.79 At1g55550 AC005223 319 178 1.79 At2g30400 U93215 311 174 1.79 At3g56400 AY039933 14429 8054 1.79 At1g76960 AF370567 591 328 1.8 At2g22790 AC005617 228 127 1.8 At1g52620 AC008016 678 377 1.8 At1g68570 AC008075 857 475 1.8 At3g43250 AL353871 211 117 1.8 At4g27900 AL035524 1215 676 1.8 At2g17190 AF360159 250 139 1.8 At4g23240 AL022347 415 231 1.8 At4g23320 AL022347 415 231 1.8 At4g23290 AL022347 415 231 1.8 At3g13010 AC024128 230 127 1.81 At4g10340 AF134129 6930 3820 1.81 At4g31630 AL031004 213 118 1.81 At5g56840 AB013392 502 278 1.81 At1g55490 AF386945 22830 12641 1.81 At3g02470 AY042824 24562 13607 1.81 At1g74310 U13949 663 365 1.82 At2g36980 AC006922 398 219 1.82 At3g17360 AB022216 296 163 1.82 At1g17150 AC007651 210 115 1.82 At4g30500 AL161577 708 388 1.82 At5g62690 M84701 554 304 1.82 At5g62700 M84701 554 304 1.82 At3g17790 AJ133747 537 294 1.83 At3g23690 AP000377 17759 9687 1.83 At3g12500 AC069474 264 144 1.83 At4g38970 AL035679 11816 6462 1.83 At1g71250 AC016162 263 144 1.83 At5g53420 AB020754 563 307 1.83 At1g70760 AC011663 236 129 1.83 At1g29600 AC068667 226 123 1.83 At5g37770 AB016873 7766 4226 1.84 At1g75950 AF059294 514 280 1.84 At1g78980 AC002986 231 126 1.84 At2g28040 AC005851 292 158 1.84 At3g01350 AC010676 345 187 1.84 At3g59630 AL138659 309 168 1.84 At1g09340 AY035050 18319 9954 1.84 At4g18100 AL110123 25024 13606 1.84 At4g23310 AL022347 225 123 1.84 At2g26840 AC005168 678 369 1.84 NoAnno F15338 312 169 1.85 At1g02400 AC064879 297 161 1.85 At2g48090 AC006072 258 140 1.85 At5g39610 AB012243 263 142 1.85 At2g31220 AC006593 477 257 1.86 At2g24300 AC006403 205 110 1.86 At5g42500 AB016888 256 137 1.86 At3g01570 AC009325 426 229 1.86 At3g05710 AJ245408 257 139 1.86 At1g07470 X98861 13725 7392 1.86 At1g07480 X98861 13725 7392 1.86 At3g14620 AB023038 519 277 1.87 At1g67920 AC012563 291 156 1.87 At1g68590 AC008075 19955 10683 1.87 At5g45850 AB016870 8826 4711 1.87 At3g62550 AY035146 23437 12503 1.87 At5g67250 AF263378 17304 9265 1.87 At2g43670 AC002333 203 108 1.88 At1g56040 AC009894 492 261 1.88 At4g05180 AF372897 5948 3170 1.88 At3g08940 AF134127 17812 9497 1.88 At5g35340 AF058826 232 123 1.88 At4g20370 AB027506 233 124 1.88 NoAnno M63234 207 110 1.89 At4g20950 AL080282 277 147 1.89 At1g31630 AC074360 573 302 1.89 At1g33070 AC074360 573 302 1.89 At4g12800 AJ245867 5393 2859 1.89 At5g14840 AL080282 277 147 1.89 At5g15240 AL353993 474 251 1.89 At4g34190 AF133716 18097 9574 1.89 At4g32260 AY042873 15062 7907 1.9 At2g43790 AV558477 440 232 1.9 At3g01440 AC010870 5091 2683 1.9 At1g02200 U40489 5410 2841 1.9 At3g22120 AF104328 22876 12056 1.9 At2g20880 AC006234 332 174 1.91 At1g31940 AC079041 207 108 1.91 At1g32470 AF385740 18411 9658 1.91 At4g08730 AL161512 403 211 1.91 At3g44320 X63445 22225 11646 1.91 At3g44300 X63445 22225 11646 1.91 At3g44310 X63445 22225 11646 1.91 At5g24210 AB006701 2109 1105 1.91 At3g16640 AY045802 1511 792 1.91 At1g76130 AC009978 868 451 1.92 At1g51140 AY034941 891 463 1.92 At1g74980 AY045856 17627 9200 1.92 At1g27270 AC004557 224 117 1.92 At1g05880 AC009999 279 146 1.92 At4g02770 AF389290 8820 4595 1.92 At1g27980 AF360166 961 499 1.92 At1g21910 AC013482 2917 1523 1.92 At5g58570 AY045817 656 339 1.93 At4g36510 AL161589 207 107 1.93 At3g58380 AL137081 266 138 1.93 At3g12810 AB024033 207 107 1.93 At2g28340 AC006283 417 215 1.94 At4g03890 AL161498 298 153 1.94 At4g02250 AL161494 201 104 1.94 NoAnno F15136 271 139 1.95 At5g02260 AL162874 306 157 1.95 At1g30060 AC022455 303 156 1.95 At2g38140 AC003028 12398 6316 1.96 At1g25988 AC084221 235 120 1.96 At1g51760 Y13577 208 106 1.96 At2g14990 AL161509 252 129 1.96 At2g46870 AC004411 19086 9748 1.96 At2g14970 AF262043 16604 8412 1.97 At1g58290 AC008051 15587 7898 1.97 At4g16080 AL161543 703 357 1.97 At5g02520 AL162971 202 103 1.97 At4g08060 AF262043 16604 8412 1.97 At3g27860 AP000371 270 137 1.97 At1g64670 AC009519 239 121 1.98 At1g26310 AF061410 275 139 1.98 At5g38730 AB011478 307 155 1.98 At1g23205 AC002311 2171 1098 1.98 At4g04640 M61741 8213 4124 1.99 At1g52220 AC022354 21605 10842 1.99 At4g02870 AL161495 273 137 1.99 At1g34740 AF104920 212 107 1.99 At2g05560 AF104920 212 107 1.99 At2g14770 AF104920 212 107 1.99 At3g24390 AF104920 212 107 1.99 At3g42730 AF104920 212 107 1.99 At4g08880 AF104920 212 107 1.99 At5g36860 AF104920 212 107 1.99 At4g24570 AY042859 3564 1794 1.99 At1g52020 AF104920 212 107 1.99 At3g15720 AB017071 423 212 1.99 At1g25886 AF104920 212 107 1.99 At3g43390 AF104920 212 107 1.99 At4g03300 AF104920 212 107 1.99 At4g05280 AF104920 212 107 1.99 At3g28610 AP000420 205 103 1.99 At3g09440 Y17053 3577 1784 2 At1g30250 AC073506 6659 3331 2 At5g36960 AB016877 271 135 2.01 At2g37220 AY048251 14320 7098 2.02 At1g71691 AC012654 288 142 2.02 At2g31980 AC006223 211 105 2.02 At2g27400 AC006233 313 154 2.03 At1g11260 X55350 17446 8597 2.03 At3g23250 Y14207 215 106 2.03 At5g53490 AF370552 19631 9694 2.03 At2g33830 AB050786 14290 7021 2.04 At4g14950 AV537413 254 124 2.04 At1g22270 AC068562 290 142 2.04 At5g35735 AF372955 4539 2220 2.04 At2g15960 AC006438 23165 11339 2.04 At2g36800 AC006282 584 287 2.04 At5g61440 AF144389 6829 3348 2.04 At1g10040 AC004122 352 173 2.04 At3g20810 AB025629 4866 2370 2.05 At2g42730 AC006931 248 121 2.05 At3g47960 AF370202 5950 2905 2.05 At2g01600 AV541295 265 129 2.06 At3g07480 AF386949 267 130 2.06 At1g56070 AC009894 26599 12925 2.06 At2g43940 AC004005 607 294 2.06 At4g04610 U53864 1154 559 2.07 At3g13340 AY048298 1955 945 2.07 At5g59220 AB016890 282 137 2.07 At2g28960 AC005315 231 112 2.07 At2g19350 AC003058 210 101 2.08 At1g21960 AC013482 298 144 2.08 At2g30860 AF372905 25890 12409 2.09 At2g45350 AC002387 585 280 2.09 At5g37640 L05363 11449 5488 2.09 At4g05320 L05363 11449 5488 2.09 At4g05050 L05363 11449 5488 2.09 At5g20620 L05363 11449 5488 2.09 At5g03240 L05363 11449 5488 2.09 At3g09790 L05363 11449 5488 2.09 At1g65350 L05363 11449 5488 2.09 At1g55060 L05363 11449 5488 2.09 At3g62250 L05363 11449 5488 2.09 At4g02890 L05363 11449 5488 2.09 At4g16690 AL161544 1258 601 2.1 At1g08640 AF370182 372 178 2.1 At2g02815 AF175994 283 134 2.1 At3g62150 AL138651 293 140 2.1 At1g56430 AC058785 641 306 2.1 At1g61370 AC004255 444 211 2.1 At3g24100 AF370331 463 220 2.1 At4g02140 AL161493 252 119 2.11 At3g46190 AL355775 210 100 2.11 At3g56260 AL163763 349 166 2.11 At2g21170 AF247559 20479 9650 2.12 At1g80280 AV547254 221 104 2.12 At3g21760 AF372973 1223 575 2.13 At1g14600 AC010657 413 193 2.14 At3g15650 AB017071 416 194 2.14 At2g25510 AC006300 14882 6928 2.15 At4g11440 AL050399 402 187 2.15 At5g03000 AL163002 249 116 2.15 At1g50560 AC012561 241 111 2.16 At3g04120 AC016829 19007 8803 2.16 At5g26000 AY045681 4323 1999 2.16 At1g15620 AC013453 277 128 2.16 At1g65400 AF325110 2725 1260 2.16 At1g55290 AC027034 243 112 2.16 At1g50540 AC012561 241 111 2.16 At3g46890 AL096859 16966 7863 2.16 At1g61400 AC004255 248 115 2.16 At1g61430 AC004255 248 115 2.16 At1g61440 AC004255 248 115 2.16 NoAnno AF003102 550 254 2.17 At3g47470 M63931 5758 2649 2.17 At4g01530 AL161492 212 98 2.17 At3g21750 AB025634 825 381 2.17 At2g18120 AC007212 258 119 2.17 At4g22020 AJ002892 3194 1468 2.18 At1g21310 AB031821 278 128 2.18 At1g49490 AJ002892 3194 1468 2.18 At4g27440 AY042883 279 128 2.18 At3g46250 AL355775 207 95 2.18 At2g40200 AF085279 212 97 2.19 At4g01310 AL161491 15461 7075 2.19 At5g65980 AB011474 204 93 2.19 At3g63290 AV543251 247 113 2.19 At5g27280 AF007271 303 139 2.19 At4g35100 AY049238 16586 7554 2.2 At2g22760 AC005617 203 92 2.2 At2g45960 AY049238 16586 7554 2.2 At2g16850 AY049238 16586 7554 2.2 At2g39310 AC004697 205 93 2.2 At3g61430 AY049238 16586 7554 2.2 At4g19700 AL024486 975 443 2.2 At2g14800 AC004705 483 219 2.21 At2g03020 AC004138 362 164 2.21 At3g60810 AL162295 261 118 2.21 At3g52145 AI995315 206 93 2.22 At2g16600 U40399 24863 11149 2.23 At2g30570 U93215 8840 3958 2.23 At3g53420 AY039579 20978 9407 2.23 At5g13510 AL391710 21808 9770 2.23 At4g35450 U70425 19189 8562 2.24 At3g61700 AV557897 238 106 2.24 At5g66570 AF372898 8498 3775 2.25 At2g46330 AC006526 18763 8298 2.26 At5g06540 AP002543 307 136 2.26 At3g15530 AC024081 1342 592 2.27 At1g20300 AC026234 653 286 2.28 At2g27385 AV531683 327 144 2.28 NoAnno AF360265 27827 12129 2.29 At1g75350 AF370226 16420 7163 2.29 At1g30260 AC073506 4248 1858 2.29 At2g32290 AC005700 434 189 2.3 At3g46430 AL133298 19794 8588 2.3 At4g16370 AL161543 3197 1382 2.31 At1g44810 AY042861 277 120 2.32 At4g17980 AL021889 357 154 2.32 At5g52050 AB015478 478 205 2.33 At3g50820 AJ145957 16012 6873 2.33 At5g42900 AB008264 7894 3370 2.34 At4g30750 AY037251 209 89 2.36 At2g31920 AC006533 210 89 2.36 At2g01300 AC006200 1094 461 2.37 At5g08280 X73535 25523 10707 2.38 At5g62300 AF370460 27616 11598 2.38 At5g50610 AB025619 222 93 2.38 At5g50710 AB025619 222 93 2.38 At3g07650 AC009176 4686 1965 2.39 At5g11780 AL163814 274 114 2.39 At4g32430 AL034567 394 164 2.4 At5g02500 X74604 20275 8429 2.41 At3g54890 AF326866 9157 3789 2.42 At3g59340 AF370505 692 284 2.43 At1g79850 Z11151 830 339 2.45 At2g21660 AY042826 613 250 2.45 At2g39320 AC004697 773 316 2.45 At2g21420 AC006841 260 106 2.45 At4g36010 AF360165 958 388 2.47 At4g13940 AF325037 26706 10790 2.48 At1g32080 AC084165 20969 8468 2.48 At4g01260 AL161491 227 91 2.48 At4g31830 AL049607 292 118 2.48 At3g24420 AP000382 8999 3623 2.48 At2g28900 AY045593 21483 8645 2.49 At1g63820 AC010852 214 86 2.5 At5g16400 AF144386 19378 7696 2.52 At1g14320 AY045866 22985 9128 2.52 At1g27710 AC012375 213 85 2.52 At1g75690 AC006434 24943 9882 2.52 At3g44990 X92975 865 343 2.52 At5g06290 AF326871 22183 8782 2.53 At3g15630 AB017071 22541 8902 2.53 At5g01100 AL137189 595 235 2.53 At1g73810 AC012679 279 110 2.54 At5g14610 AL163792 30717 12004 2.56 At5g42530 AB016888 7812 3054 2.56 At2g28800 U89272 22626 8809 2.57 At2g36970 AC006922 308 120 2.57 At1g77110 AC002291 255 99 2.58 At1g28410 AC010155 257 99 2.6 At1g32990 AF325023 20190 7763 2.6 At5g63580 AB005234 209 80 2.62 At2g21800 AC007019 204 78 2.63 At2g33450 AC002332 25052 9518 2.63 At2g23910 AC005170 699 266 2.63 At2g19150 AC002392 206 78 2.64 At5g23660 AF095641 2931 1106 2.65 At3g21470 AB019232 401 151 2.66 At5g13630 Z68495 21783 8155 2.67 At2g42220 AY045616 20113 7535 2.67 At2g03190 AC005313 206 77 2.68 At1g44880 AC020576 245 91 2.68 At2g10350 AC020576 245 91 2.68 At4g03970 AC020576 245 91 2.68 At3g42530 AC020576 245 91 2.68 At3g01310 AC010676 212 79 2.68 At3g45680 AL157735 258 95 2.72 At3g45690 AL157735 258 95 2.72 At2g10940 AC006429 8529 3119 2.73 At5g46110 AY037211 7130 2614 2.73 At2g41430 AC004625 8374 3041 2.75 At1g48300 AC007932 2604 935 2.78 At1g28760 AC007508 310 111 2.8 At1g44040 AC022314 360 129 2.8 At1g08790 AC003981 277 99 2.81 At5g63090 AB008265 223 80 2.81 At3g49910 AF370158 22291 7877 2.83 At3g12840 AB024033 220 77 2.84 At2g29280 AC004561 496 175 2.84 At1g12610 AC025417 293 103 2.85 At2g28460 AC006587 256 89 2.86 At2g38240 AC003028 282 98 2.87 At2g05070 AY045787 20173 6958 2.9 At2g05100 AY045787 20173 6958 2.9 At4g25050 T45818 15045 5121 2.94 At4g10260 AL049488 309 105 2.94 At1g49500 AF370563 22168 7513 2.95 At5g58310 AB019228 1438 487 2.95 At3g45520 AL161500 215 72 2.97 At4g04380 AL161500 215 72 2.97 At3g25290 AB026647 307 103 2.99 At3g01500 AC009325 616 205 3 At4g24420 AL078637 202 67 3 At3g43600 AB005805 19762 6576 3.01 At5g11370 AL360314 236 78 3.01 At2g28000 AC006929 27972 9297 3.01 At5g39670 AB012243 291 96 3.03 At5g24780 AF386930 375 123 3.05 At1g23310 AF360195 31336 10247 3.06 At2g34420 X64460 7379 2403 3.07 At3g21640 AJ224640 20590 6686 3.08 At5g15960 X55053 22316 7183 3.11 At5g15970 X55053 22316 7183 3.11 At3g01600 AC009325 233 75 3.11 At4g32540 AL050398 303 97 3.12 At2g11820 AB047398 207 66 3.12 At4g17350 AL161546 215 69 3.13 At1g04270 AY048221 22066 7025 3.14 At2g17180 AC007127 345 109 3.15 At4g21280 AL021960 7348 2313 3.18 At3g53290 AL132958 228 71 3.2 At5g44980 AB010693 210 65 3.22 At2g30950 AF135189 29571 9161 3.23 At3g12430 AC069474 270 83 3.24 At4g32490 AL034567 261 81 3.25 At1g69990 AC002062 249 76 3.26 At5g05250 AB010692 1176 358 3.28 At3g56360 AL163972 1291 391 3.3 At1g72150 AY045913 24133 7291 3.31 At4g21990 U53865 1684 509 3.31 At2g30840 AC004669 308 93 3.32 At1g41810 AC022456 240 71 3.37 At5g29090 AC022456 240 71 3.37 At5g32610 AC022456 240 71 3.37 At3g59170 AL356014 217 64 3.41 At5g37470 AP000607 223 65 3.45 At2g25040.a AV558611 287 83 3.46 At3g32370.a AV558611 287 83 3.46 At5g37300 AB017069 753 217 3.48 At4g22214 AL021712 256 73 3.51 At1g48700 AC073555 275 78 3.52 At1g55850 AC002304 267 75 3.57 At1g04920 AC004809 362 99 3.64 At4g03280 AJ243702 1486 400 3.71 At1g35660.a AC007887 203 55 3.73 At4g27110 AL035680 201 51 3.9 At2g04820 AC006955 341 85 4.01 At1g75910 AC007396 205 51 4.04 At3g21980 AB028622 215 52 4.15 At3g27830 AP000371 25310 6009 4.21 At1g74080 AC016662 352 83 4.26 At2g17850 AC003952 277 65 4.29 At2g45570 AC003680 251 58 4.33 At3g56040 AV548493 280 62 4.49 At5g25980 AF360348 28538 6306 4.53 At3g43580 AL391734 222 48 4.61 At5g38710 AB011478 376 78 4.81 At3g12760 AB024033 271 50 5.41 At1g32920.a BE522104 235 28 8.35 W, wild type; M, mutant. 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The invention claimed is:
 1. A method for altering plant growth, comprising introducing and expressing in a plant a nucleic acid encoding a plant UBiquitin-Specific Protease 15 (UBP15) polypeptide comprising the following motifs: (i) a Cysteine box (Cys box); (ii) a Histidine box (His box); and (iii) a ZnMYND zinc finger domain, wherein said nucleic acid is selected from the group consisting of: (a) a nucleic acid comprising the nucleotide sequence of SEQ ID NO: 1; (b) a nucleic acid encoding a polypeptide comprising the amino acid sequence of SEQ ID NO: 2; and (c) a nucleic acid encoding a polypeptide having at least 95% sequence identity to the amino acid sequence of SEQ ID NO: 2, wherein said polypeptide has de-ubiquitination activity in vitro, and wherein said plant has one or more of the following: increased number of rosette leaves, increased flowering time, increased fresh weight of rosette leaves, increased silique length, increased root length, increased primary stem length, and/or increased primary stem diameter relative to a control plant.
 2. The method of claim 1, wherein said nucleic acid is operably linked to a constitutive promoter.
 3. A plant having increased number of rosette leaves, increased flowering time, increased fresh weight of rosette leaves, increased silique length, increased root length, increased primary stem length, and/or increased primary stem diameter relative to a control plant, wherein the increased number of rosette leaves, increased flowering time, increased fresh weight of rosette leaves, increased silique length, increased root length, increased primary stem length, and/or increased primary stem diameter is obtained by the method of claim
 1. 4. A construct comprising: (i) a nucleic acid encoding a plant UBiquitin-Specific Protease 15 (UBP15) polypeptide comprising the following motifs: a) a Cysteine box (Cys box); b) a Histidine box (His box); and c) a ZnMYND zinc finger domain, wherein said nucleic acid is selected from the group consisting of: (a) a nucleic acid comprising the nucleotide sequence of SEQ ID NO: 1; (b) a nucleic acid encoding a polypeptide comprising the amino acid sequence of SEQ ID NO: 2; and (c) a nucleic acid encoding a polypeptide having at least 95% sequence identity to the amino acid sequence of SEQ ID NO: 2, wherein said polypeptide has de-ubiquitination activity in vitro; (ii) one or more heterologous control sequences capable of driving expression of the nucleic acid of (i); and optionally (iii) a transcription termination sequence, wherein expression of said nucleic acid in a plant confers one or more of the following: increased number of rosette leaves, increased flowering time, increased fresh weight of rosette leaves, increased silique length, increased root length, increased primary stem length, and/or increased primary stem diameter relative to a control plant.
 5. The construct of claim 4, wherein one of said heterologous control sequences is a constitutive promoter.
 6. A method for making a plant having altered growth relative to a control plant, comprising transforming a plant cell with the construct of claim 4 and regenerating a plant from the plant cell, wherein said plant has increased expression of said nucleic acid and has one or more of the following: increased number of rosette leaves, increased flowering time, increased fresh weight of rosette leaves, increased silique length, increased root length, increased primary stem length, and/or increased primary stem diameter relative to a control plant.
 7. A method for the production of a transgenic plant having altered growth relative to a control plant, comprising: (i) introducing and expressing in a plant or plant cell a nucleic acid encoding a plant UBiquitin-Specific Protease 15 (UBP15) comprising the following motifs: (a) a Cysteine box (Cys box); (b) a Histidine box (His box); and (c) a ZnMYND zinc finger domain; and (ii) cultivating the plant or plant cell under conditions promoting plant growth and development, wherein said nucleic acid is selected from the group consisting of: (a) a nucleic acid comprising the nucleotide sequence of SEQ ID NO: 1; (b) a nucleic acid encoding a polypeptide comprising the amino acid sequence of SEQ ID NO: 2; and (c) a nucleic acid encoding a polypeptide having at least 95% sequence identity to the amino acid sequence of SEQ ID NO: 2, wherein said polypeptide has de-ubiquitination activity in vitro, wherein said plant or plant cell has increased expression of said nucleic acid, and wherein said plant has one or more of the following: increased number of rosette leaves, increased flowering time, increased fresh weight of rosette leaves, increased silique length, increased root length, increased primary stem length, and/or increased primary stem diameter relative to a control plant.
 8. A transgenic plant having an increase in one or more of rosette leaves, flowering time, fresh weight of rosette leaves, silique length, root length, primary stem length, and/or primary stem diameter relative to a control plant, wherein said increase results from introducing and expressing in said plant a nucleic acid encoding a plant UBP15 polypeptide comprising: (a) a Cysteine box (Cys box); (b) a Histidine box (His box); and (c) a ZnMYND zinc finger domain, wherein said nucleic acid is selected from the group consisting of: (a) a nucleic acid comprising the nucleotide sequence of SEQ ID NO: 1; (b) a nucleic acid encoding a polypeptide comprising the amino acid sequence of SEQ ID NO: 2; and (c) a nucleic acid encoding a polypeptide having at least 95% sequence identity to the amino acid sequence of SEQ ID NO: 2, wherein said polypeptide has de-ubiquitination activity in vitro.
 9. The plant of claim 3, wherein said plant is a crop plant.
 10. Harvestable parts of the plant of claim 9, wherein said harvestable parts comprise the nucleic acid encoding the UBP15 polypeptide, and wherein said harvestable parts comprise shoot biomass and/or seeds.
 11. The method of claim 1, wherein said nucleic acid encoding a plant UBP15 polypeptide is from a dicotyledonous plant.
 12. The plant of claim 3, wherein said plant is rice, maize, wheat, barley, millet, rye, triticale, sorghum, or oats.
 13. A plant, plant part, plant cell, or progeny thereof comprising the construct of claim 4, wherein the plant, a plant generated from the plant part or plant cell, or the progeny has one or more of the following: increased number of rosette leaves, increased flowering time, increased fresh weight of rosette leaves, increased silique length, increased root length, increased primary stem length, and/or increased primary stem diameter relative to a control plant.
 14. The plant of claim 3, wherein said plant is a monocot.
 15. The plant of claim 3, wherein said plant is a cereal.
 16. The method of claim 1, wherein said nucleic acid comprises the nucleotide sequence of SEQ ID NO: 1 or encodes a polypeptide comprising the amino acid sequence of SEQ ID NO:
 2. 17. The construct of claim 4, wherein said nucleic acid comprises the nucleotide sequence of SEQ ID NO: 1 or encodes a polypeptide comprising the amino acid sequence of SEQ ID NO:
 2. 18. The method of claim 7, wherein said nucleic acid comprises the nucleotide sequence of SEQ ID NO: 1 or encodes a polypeptide comprising the amino acid sequence of SEQ ID NO:
 2. 19. The transgenic plant of claim 8, wherein said nucleic acid comprises the nucleotide sequence of SEQ ID NO: 1 or encodes a polypeptide comprising the amino acid sequence of SEQ ID NO:
 2. 20. A plant part or seed of the plant of claim 3, wherein said plant part or seed comprises the nucleic acid encoding the UBP15 polypeptide. 